| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33314056-33314119 | Common:2; Rare:21 | ||||
| chr6:33314227-33314542 | Common:3; Rare:47 | ||||
| chr6:33322893-33323265 | Common:5; Rare:115 | ||||
| chr6:33391489-33391906 | Common:3; Rare:99 | ||||
| chr6:33417898-33418044 | Rare:57 | ||||
| chr6:33418048-33418495 | Common:3; Rare:107 | ||||
| chr6:33454429-33454593 | Rare:43 | ||||
| chr6:33580204-33580349 | Common:2; Rare:40 | ||||
| chr6:34236752-34236914 | Common:2; Rare:64 | ||||
| chr6:34248977-34249218 | Rare:54 | ||||
| chr6:34392386-34392657 | Rare:97 | ||||
| chr6:34426019-34426216 | Common:5; Rare:85; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696611-34696988 | Common:1; Rare:98 | ||||
| chr6:34757380-34757550 | Rare:53 | ||||
| chr6:34791903-34792122 | Common:3; Rare:66 |