| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30589689-30589905 | Rare:60 | ||||
| chr6:30617224-30617462 | Common:1; Rare:67 | ||||
| chr6:30617756-30617908 | Rare:69 | ||||
| chr6:30647319-30647440 | Common:2; Rare:39 | ||||
| chr6:30686611-30686800 | Common:2; Rare:37 | ||||
| chr6:30687139-30687453 | Rare:61 | ||||
| chr6:30717243-30717437 | Common:1; Rare:40 | ||||
| chr6:30720124-30720555 | Common:1; Rare:99 | ||||
| chr6:30742609-30743096 | Common:2; Rare:99 | ||||
| chr6:30744248-30744462 | Rare:50 | ||||
| chr6:30883182-30883306 | Rare:17 | ||||
| chr6:30886174-30886370 | Common:1; Rare:33 | ||||
| chr6:30908014-30908237 | Common:2; Rare:44 | ||||
| chr6:30914160-30914370 | Rare:76; Clinvar (benign):2 | ||||
| chr6:31158174-31158597 | Common:8; Rare:107 |