Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114716674-114716917 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):2 | ||||
chr1:114757415-114757743 | Common:1; Rare:68 | ||||
chr1:114757933-114758202 | Common:3; Rare:82 | ||||
chr1:114780404-114780806 | Common:1; Rare:142 | ||||
chr1:115089464-115089616 | Common:2; Rare:57 | ||||
chr1:115642630-115643240 | Common:7; Rare:122 | ||||
chr1:116373077-116373331 | Rare:80 | ||||
chr1:116373880-116374030 | Common:1; Rare:43 | ||||
chr1:116570357-116570590 | Rare:53 | ||||
chr1:116570978-116571164 | Common:2; Rare:55 | ||||
chr1:116667659-116667899 | Common:2; Rare:87 | ||||
chr1:116909713-116910100 | Common:1; Rare:111 | ||||
chr1:117059889-117060372 | Common:7; Rare:125 | ||||
chr1:117093000-117093520 | Common:1; Rare:70 | ||||
chr1:117121695-117122030 | Common:1; Rare:107 |