| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827989-102828151 | Common:1; Rare:60 | ||||
| chr4:102868873-102869063 | Common:2; Rare:61 | ||||
| chr4:105708654-105708827 | Rare:55 | ||||
| chr4:106316178-106316593 | Common:5; Rare:132 | ||||
| chr4:107720166-107720504 | Common:7; Rare:137 | ||||
| chr4:107824597-107824735 | Rare:30 | ||||
| chr4:107989679-107989919 | Common:6; Rare:113; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620380-108620647 | Common:6; Rare:135 | ||||
| chr4:109703412-109703606 | Common:1; Rare:59 | ||||
| chr4:109815464-109815544 | Rare:25 | ||||
| chr4:110622745-110622940 | Common:3; Rare:40 | ||||
| chr4:112231592-112231831 | Common:2; Rare:74 | ||||
| chr4:112297143-112297412 | Common:1; Rare:41 | ||||
| chr4:112636875-112637187 | Common:1; Rare:86 | ||||
| chr4:112637394-112637570 | Common:3; Rare:47 |