| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241198224-241198419 | Common:1; Rare:35 | ||||
| chr2:241200882-241201066 | Common:2; Rare:42 | ||||
| chr2:241215364-241215677 | Common:4; Rare:51 | ||||
| chr2:241235523-241235831 | Rare:80 | ||||
| chr2:241252968-241253091 | Rare:40 | ||||
| chr2:241902577-241902837 | Common:2; Rare:52 | ||||
| chr2:242026154-242026411 | Common:1; Rare:46 | ||||
| chr20:5445713-5445852 | Rare:23 | ||||
| chr20:15699627-15699864 | Common:3; Rare:48 | ||||
| chr20:18793869-18794096 | Rare:60 | ||||
| chr20:19757512-19757668 | Common:3; Rare:44 | ||||
| chr20:19757927-19758276 | Common:5; Rare:120 | ||||
| chr20:23358098-23358242 | Common:1; Rare:41 | ||||
| chr20:25290349-25290612 | Common:3; Rare:97 | ||||
| chr20:25292241-25292549 | Common:3; Rare:126; Clinvar (pathogenic):1 |