| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144790348-144790550 | Common:3; Rare:63 | ||||
| chr8:144792305-144792585 | Common:3; Rare:109 | ||||
| chr8:144798713-144798922 | Common:3; Rare:74 | ||||
| chr8:144827201-144827608 | Common:2; Rare:117 | ||||
| chr8:144852855-144853173 | Common:1; Rare:102 | ||||
| chr8:144901406-144901734 | Common:1; Rare:92 | ||||
| chr8:145052208-145052497 | Common:10; Rare:83 | ||||
| chr9:2621685-2621814 | Rare:56; Clinvar:1 | ||||
| chr9:2844043-2844340 | Common:5; Rare:111 | ||||
| chr9:3525863-3526130 | Common:1; Rare:113 | ||||
| chr9:4299966-4300269 | Common:5; Rare:113; Clinvar (benign):1 | ||||
| chr9:4662268-4662415 | Common:5; Rare:64 | ||||
| chr9:4662772-4663143 | Rare:147 | ||||
| chr9:4679434-4679707 | Rare:120 | ||||
| chr9:4679830-4679908 | Common:1; Rare:34 |