Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100274350-100274582 | Rare:49 | ||||
chr1:100279291-100279602 | Common:2; Rare:53 | ||||
chr1:100289798-100289811 | Rare:2 | ||||
chr1:100394020-100394030 | Rare:1 | ||||
chr1:100926894-100927151 | Common:1; Rare:56 | ||||
chr1:101492249-101492418 | Common:2; Rare:32 | ||||
chr1:103550670-103550982 | Rare:65 | ||||
chr1:107570825-107570869 | Rare:9 | ||||
chr1:107570906-107571207 | Common:4; Rare:77 | ||||
chr1:108325104-108325162 | Rare:5 | ||||
chr1:108695712-108696079 | Rare:64 | ||||
chr1:108696080-108696385 | Common:1; Rare:66 | ||||
chr1:108808589-108809041 | Common:1; Rare:96 | ||||
chr1:108884502-108884642 | Common:1; Rare:29 | ||||
chr1:108923811-108924146 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 |