| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33299417-33299518 | Common:1; Rare:25 | ||||
| chr6:33322683-33322740 | Rare:7 | ||||
| chr6:33322891-33323340 | Common:5; Rare:141 | ||||
| chr6:33391297-33391927 | Common:4; Rare:135 | ||||
| chr6:33417862-33417952 | Rare:38 | ||||
| chr6:33417957-33418508 | Common:3; Rare:141 | ||||
| chr6:33420043-33420301 | Rare:53; Clinvar (benign):1 | ||||
| chr6:33454383-33454604 | Rare:65 | ||||
| chr6:33580175-33580339 | Common:2; Rare:47 | ||||
| chr6:33711439-33711540 | Common:1; Rare:43 | ||||
| chr6:33711625-33711790 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr6:33789126-33789253 | Common:1; Rare:60 | ||||
| chr6:34236749-34236939 | Common:3; Rare:76 | ||||
| chr6:34248977-34249220 | Rare:55 | ||||
| chr6:34392348-34392749 | Rare:152 |