| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43824179-43824579 | Rare:173 | ||||
| chr15:43824491-43825010 | Common:14; Rare:553 | ||||
| chr15:43826751-43827151 | Common:2; Rare:539 | ||||
| chr15:44194461-44195022 | Common:2; Rare:282 | ||||
| chr15:44288200-44288986 | Common:155; Rare:1323 | ||||
| chr15:44288959-44289428 | Common:4; Rare:173 | ||||
| chr15:44426780-44427370 | Common:7; Rare:850 | ||||
| chr15:44427360-44427770 | Common:5; Rare:316 | ||||
| chr15:44428006-44428506 | Common:4; Rare:191 | ||||
| chr15:44536290-44536570 | Common:1; Rare:57 | ||||
| chr15:44536590-44537427 | Common:18; Rare:1313 | ||||
| chr15:44537581-44537981 | Common:2; Rare:131 | ||||
| chr15:44551230-44551700 | Rare:98 | ||||
| chr15:44555022-44555422 | Common:6; Rare:142 | ||||
| chr15:44565452-44566656 | Common:5; Rare:434; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):5 |