| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30647098-30647189 | Common:1; Rare:29 | ||||
| chr6:30647303-30647565 | Common:5; Rare:87 | ||||
| chr6:30686592-30686779 | Common:2; Rare:37 | ||||
| chr6:30717261-30717449 | Common:1; Rare:41 | ||||
| chr6:30720128-30720555 | Common:1; Rare:97 | ||||
| chr6:30742474-30743069 | Common:3; Rare:127 | ||||
| chr6:30744255-30744394 | Rare:36 | ||||
| chr6:30882726-30883005 | Common:2; Rare:32 | ||||
| chr6:30908014-30908235 | Common:2; Rare:44 | ||||
| chr6:30914138-30914370 | Rare:85; Clinvar (benign):2 | ||||
| chr6:31158165-31158597 | Common:8; Rare:110 | ||||
| chr6:31197683-31197768 | Common:3; Rare:20 | ||||
| chr6:31269964-31270415 | Common:55; Rare:141 | ||||
| chr6:31271994-31272234 | Common:15; Rare:54 | ||||
| chr6:31357008-31357339 | Common:34; Rare:80 |