| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113390126-113390836 | Common:9; Rare:568 | ||||
| chr1:113758540-113759360 | Common:7; Rare:455 | ||||
| chr1:113759391-113760049 | Common:15; Rare:476 | ||||
| chr1:113811334-113812121 | Common:3; Rare:355 | ||||
| chr1:113812138-113812719 | Common:18; Rare:1056 | ||||
| chr1:113871517-113871917 | Rare:125 | ||||
| chr1:113904186-113904586 | Common:1; Rare:85 | ||||
| chr1:113904522-113904680 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:113904694-113905459 | Common:39; Rare:1067; Clinvar (benign):9 | ||||
| chr1:113928447-113929093 | Common:9; Rare:148 | ||||
| chr1:113929071-113929910 | Common:22; Rare:1012 | ||||
| chr1:113929920-113930260 | Common:2; Rare:199 | ||||
| chr1:113930210-113930462 | Common:1; Rare:170 | ||||
| chr1:113930405-113931546 | Common:10; Rare:511 | ||||
| chr1:114510140-114511820 | Common:38; Rare:1481 |