| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237361124-237361434 | Common:2; Rare:69; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:53623508-53623581 | Rare:18 | ||||
| chr21:33761781-33761986 | Common:2; Rare:49 | ||||
| chr22:22298026-22298196 | Common:6; Rare:75 | ||||
| chr22:24243717-24243836 | Common:1; Rare:23 | ||||
| chr22:29481031-29481125 | Rare:40 | ||||
| chr22:30969052-30969278 | Common:2; Rare:64 | ||||
| chr22:46069861-46070056 | Rare:43 | ||||
| chr3:40453171-40453460 | Common:5; Rare:63 | ||||
| chr3:75435060-75435345 | Common:3; Rare:103 | ||||
| chr3:101676308-101676468 | Rare:52 | ||||
| chr3:107240643-107240729 | Rare:39 | ||||
| chr3:111802380-111802610 | Common:1; Rare:26 | ||||
| chr3:112640342-112640484 | Common:1; Rare:25 | ||||
| chr3:156817029-156817335 | Rare:85 |