| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181261914-181262094 | Rare:48 | ||||
| chr5:181265612-181265671 | Rare:11 | ||||
| chr6:710932-711070 | Common:2; Rare:31 | ||||
| chr6:1554989-1555311 | Common:2; Rare:81 | ||||
| chr6:1611468-1611553 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:1686153-1686409 | Common:2; Rare:56 | ||||
| chr6:1802550-1802686 | Rare:29 | ||||
| chr6:2534689-2534990 | Common:2; Rare:58 | ||||
| chr6:2534993-2535072 | Common:1; Rare:17 | ||||
| chr6:2634408-2634781 | Common:5; Rare:87 | ||||
| chr6:2726349-2726376 | Rare:4 | ||||
| chr6:2764038-2764097 | Rare:18 | ||||
| chr6:2764304-2764389 | Rare:31 | ||||
| chr6:2764404-2764769 | Common:6; Rare:111 | ||||
| chr6:2793586-2793614 | Rare:4 |