| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30914163-30914387 | Rare:77; Clinvar (benign):2 | ||||
| chr6:31114657-31114862 | Common:4; Rare:48 | ||||
| chr6:31158131-31158705 | Common:18; Rare:260 | ||||
| chr6:31197370-31198230 | Common:35; Rare:292 | ||||
| chr6:31269000-31269320 | Common:20; Rare:75 | ||||
| chr6:31272041-31272271 | Common:30; Rare:70 | ||||
| chr6:31357145-31357331 | Common:32; Rare:53 | ||||
| chr6:31399742-31400094 | Common:10; Rare:89 | ||||
| chr6:31403300-31403750 | Common:15; Rare:170 | ||||
| chr6:31494430-31494956 | Common:18; Rare:122 | ||||
| chr6:31497850-31498220 | Common:23; Rare:106 | ||||
| chr6:31541751-31542710 | Common:17; Rare:412 | ||||
| chr6:31547427-31547738 | Common:4; Rare:161 | ||||
| chr6:31582290-31582710 | Common:1; Rare:99 | ||||
| chr6:31620269-31620854 | Common:2; Rare:342 |