Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:107529322-107529519 | Common:1; Rare:40 | ||||
chr2:108304359-108304549 | Common:1; Rare:32 | ||||
chr2:108489669-108489901 | Common:1; Rare:44 | ||||
chr2:113239796-113240019 | Rare:42 | ||||
chr2:113268480-113268672 | Rare:29 | ||||
chr2:113274690-113274803 | Rare:21 | ||||
chr2:113275959-113276056 | Rare:16 | ||||
chr2:113542685-113542821 | Common:3; Rare:13 | ||||
chr2:113584028-113584118 | Rare:20 | ||||
chr2:121529891-121530181 | Common:2; Rare:69 | ||||
chr2:131682358-131682550 | Common:3; Rare:57 | ||||
chr2:132347332-132347503 | Common:1; Rare:42 | ||||
chr2:144396413-144396825 | Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
chr2:144488930-144488978 | Rare:11 | ||||
chr2:152498879-152498910 | Rare:5 |