| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232550555-232550716 | Rare:59 | ||||
| chr2:241315173-241315298 | Common:1; Rare:43 | ||||
| chr2:241315649-241315964 | Common:5; Rare:122 | ||||
| chr20:1118478-1118627 | Common:2; Rare:46 | ||||
| chr20:1393012-1393240 | Common:2; Rare:97 | ||||
| chr20:4686209-4686475 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5950522-5950677 | Common:8; Rare:41 | ||||
| chr20:21303261-21303379 | Rare:54 | ||||
| chr20:31722851-31722963 | Rare:28 | ||||
| chr20:34112177-34112423 | Rare:73 | ||||
| chr20:34516312-34516443 | Common:3; Rare:46 | ||||
| chr20:35699344-35699466 | Rare:40 | ||||
| chr20:38033421-38033767 | Common:2; Rare:100 | ||||
| chr20:44187140-44187373 | Common:1; Rare:48 | ||||
| chr20:44966444-44966520 | Rare:25 |