| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112542139-112542489 | Common:1; Rare:111 | ||||
| chr2:112584388-112584633 | Common:1; Rare:66 | ||||
| chr2:112645713-112645953 | Common:1; Rare:89 | ||||
| chr2:112764561-112764765 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr2:112784483-112784658 | Rare:38 | ||||
| chr2:113627041-113627314 | Common:4; Rare:80 | ||||
| chr2:113756608-113756792 | Common:3; Rare:71 | ||||
| chr2:113889709-113890165 | Common:8; Rare:152 | ||||
| chr2:118014006-118014177 | Common:2; Rare:104 | ||||
| chr2:118088346-118088526 | Common:1; Rare:54 | ||||
| chr2:119366779-119367065 | Common:1; Rare:86 | ||||
| chr2:119431731-119431862 | Common:3; Rare:33 | ||||
| chr2:119678960-119679222 | Common:5; Rare:71 | ||||
| chr2:119759748-119759801 | Rare:9 | ||||
| chr2:121530579-121530884 | Common:7; Rare:127 |