Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112956095-112956495 | Common:5; Rare:152; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073059-113073246 | Common:1; Rare:71 | ||||
chr1:113904873-113905385 | Common:7; Rare:151; Clinvar (benign):1 | ||||
chr1:113929512-113929871 | Common:4; Rare:92 | ||||
chr1:114581601-114581843 | Rare:97 | ||||
chr1:114716662-114716985 | Common:4; Rare:123; Clinvar:5; Clinvar (benign):3 | ||||
chr1:114780584-114780729 | Rare:55 | ||||
chr1:116373463-116373521 | Common:1; Rare:14 | ||||
chr1:117368253-117368472 | Rare:59 | ||||
chr1:117929567-117929814 | Common:4; Rare:76 | ||||
chr1:119140628-119140735 | Rare:32 | ||||
chr1:145823882-145824265 | Rare:136 | ||||
chr1:145918665-145919034 | Common:2; Rare:88; Clinvar:1 | ||||
chr1:145927482-145927653 | Rare:43 | ||||
chr1:145964461-145964761 | Rare:64 |