| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49960266-49960503 | Common:3; Rare:87 | ||||
| chr22:49960684-49960786 | Common:1; Rare:56 | ||||
| chr22:50085200-50085640 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50169990-50170975 | Common:5; Rare:410 | ||||
| chr22:50200739-50201061 | Common:5; Rare:116 | ||||
| chr22:50244947-50245139 | Common:2; Rare:72 | ||||
| chr22:50251223-50251477 | Common:2; Rare:87 | ||||
| chr22:50261620-50261980 | Common:4; Rare:111 | ||||
| chr22:50269974-50270190 | Common:2; Rare:59 | ||||
| chr22:50270270-50270560 | Common:2; Rare:80 | ||||
| chr22:50288663-50289067 | Common:2; Rare:185 | ||||
| chr22:50326929-50327245 | Common:3; Rare:107 | ||||
| chr22:50343174-50343378 | Common:2; Rare:86 | ||||
| chr22:50475005-50475247 | Common:5; Rare:75 | ||||
| chr22:50525509-50525789 | Common:5; Rare:155; Clinvar:5; Clinvar (benign):6 |