| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:23566053-23566481 | Common:2; Rare:550; Clinvar (pathogenic):4 | ||||
| chr15:23687210-23687540 | Common:1; Rare:112 | ||||
| chr15:25437962-25438690 | Common:8; Rare:583; Clinvar (benign):3 | ||||
| chr15:25438917-25439430 | Common:21; Rare:849 | ||||
| chr15:26629030-26629460 | Common:20; Rare:505 | ||||
| chr15:28099245-28099651 | Common:16; Rare:459; Clinvar:4 | ||||
| chr15:28737550-28738157 | Common:7; Rare:444 | ||||
| chr15:28885226-28886250 | Common:20; Rare:680 | ||||
| chr15:28886250-28886940 | Common:11; Rare:276 | ||||
| chr15:29269540-29270030 | Common:17; Rare:871 | ||||
| chr15:29821446-29821661 | Rare:92 | ||||
| chr15:29821653-29822053 | Common:4; Rare:310 | ||||
| chr15:29822029-29822742 | Common:8; Rare:701 | ||||
| chr15:30625510-30626220 | Common:25; Rare:491 | ||||
| chr15:30626207-30627028 | Common:4; Rare:398 |