| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144012629-144012883 | Common:2; Rare:65 | ||||
| chr8:144078519-144078718 | Common:1; Rare:59 | ||||
| chr8:144137621-144137817 | Common:1; Rare:57 | ||||
| chr8:144148561-144148668 | Rare:22 | ||||
| chr8:144428495-144428638 | Common:2; Rare:52 | ||||
| chr8:144508997-144509106 | Rare:32 | ||||
| chr8:144529051-144529267 | Common:4; Rare:78 | ||||
| chr8:144792365-144792561 | Common:2; Rare:71 | ||||
| chr8:144827248-144827587 | Common:1; Rare:85 | ||||
| chr8:144901428-144901613 | Common:1; Rare:56 | ||||
| chr8:145052159-145052487 | Common:11; Rare:82 | ||||
| chr9:214723-214874 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:2015071-2015384 | Common:3; Rare:92 | ||||
| chr9:2844051-2844382 | Common:7; Rare:129 | ||||
| chr9:3525772-3526120 | Common:1; Rare:129 |