Association between HMGCR, CRP, and CETP gene polymorphisms and metabolic/inflammatory serum profile in healthy adolescents

Table 3 List of the non-coding SNPs and related RegulomeDB scores

dbSNP IDs	Chromosome location	Rank	Score
rs3846663	chr5:74655725–74655726	1f	0.55324
rs3024509	chr1:206943296–206943297	3a	0.55134
rs5030708	chr16:56996278–56996279	3a	0.47027
rs142563098	chr5:74633013–74633014	4	0.60906
rs1417938	chr1:159684185–159684186	5	0.58955
rs7481842	chr11:61639704–61639705	5	0.13454
rs1130864	chr1:159683090–159683091	7	0.18412

RegulomeDb category summaries [33]. Rank refers to the supporting evidence for that particular location or variant id. In general, if more supporting data is available, the higher is its likelihood of being functional and hence receives a higher score (with 1 being higher and 7 being lower score); 1b-1f: Likely to affect binding and linked to expression of a gene target; 2a-2c: Likely to affect binding; 3a-3b: Less likely to affect binding;4-5-6: Minimal binding evidence
The RegulomeDB probability score is ranging from 0 to 1, with 1 being most likely to be a regulatory variant

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