| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11364990-11365300 | Common:9; Rare:62 | ||||
| chr2:11365250-11365667 | Common:6; Rare:104 | ||||
| chr2:11483380-11483580 | Common:2; Rare:49 | ||||
| chr2:11483580-11484060 | Common:8; Rare:217 | ||||
| chr2:11498089-11498336 | Rare:36 | ||||
| chr2:11499220-11499470 | Common:1; Rare:54 | ||||
| chr2:11681272-11681460 | Rare:41 | ||||
| chr2:11744050-11744371 | Common:1; Rare:119 | ||||
| chr2:11819240-11819670 | Common:2; Rare:166; Clinvar (pathogenic):2 | ||||
| chr2:11830132-11830512 | Common:2; Rare:74 | ||||
| chr2:13531440-13532170 | Common:18; Rare:193 | ||||
| chr2:13532872-13533315 | Common:13; Rare:181 | ||||
| chr2:13533260-13533660 | Common:3; Rare:127 | ||||
| chr2:13538130-13538390 | Common:8; Rare:101 | ||||
| chr2:17543979-17544163 | Common:2; Rare:59 |