| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106629470-106629649 | Common:3; Rare:41 | ||||
| chr6:107459046-107459068 | Rare:7 | ||||
| chr6:107958048-107958421 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:109440604-109440911 | Common:2; Rare:102 | ||||
| chr6:109455673-109456063 | Common:3; Rare:106 | ||||
| chr6:109691151-109691326 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110874609-110874813 | Common:4; Rare:65 | ||||
| chr6:111483133-111483597 | Common:1; Rare:165 | ||||
| chr6:111605805-111606118 | Common:2; Rare:59 | ||||
| chr6:112087461-112087684 | Rare:65 | ||||
| chr6:113970966-113971427 | Common:4; Rare:169 | ||||
| chr6:116100723-116100886 | Rare:59 | ||||
| chr6:116254046-116254210 | Common:2; Rare:47 | ||||
| chr6:116279850-116280108 | Common:2; Rare:86 | ||||
| chr6:116571201-116571510 | Common:1; Rare:79 |