| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111139270-111139559 | Common:2; Rare:56 | ||||
| chr1:111139792-111139889 | Rare:14 | ||||
| chr1:111140036-111140305 | Common:2; Rare:93 | ||||
| chr1:111619551-111619918 | Common:2; Rare:112 | ||||
| chr1:111739360-111739560 | Common:2; Rare:51 | ||||
| chr1:112396003-112396272 | Common:1; Rare:84 | ||||
| chr1:112619102-112619236 | Rare:48 | ||||
| chr1:112619642-112619842 | Common:1; Rare:70 | ||||
| chr1:112707080-112707246 | Rare:60 | ||||
| chr1:112956178-112956467 | Common:5; Rare:126; Clinvar:9; Clinvar (benign):3 | ||||
| chr1:113073076-113073252 | Common:1; Rare:69 | ||||
| chr1:113390209-113390532 | Common:1; Rare:81 | ||||
| chr1:113759517-113759630 | Common:1; Rare:36 | ||||
| chr1:113812273-113812579 | Common:2; Rare:121 | ||||
| chr1:113904831-113905365 | Common:5; Rare:158; Clinvar (benign):1 |