| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33271646-33272131 | Common:3; Rare:173 | ||||
| chr6:33289195-33289348 | Common:1; Rare:40 | ||||
| chr6:33299266-33299510 | Common:2; Rare:56 | ||||
| chr6:33417866-33417959 | Rare:40 | ||||
| chr6:33418080-33418423 | Common:2; Rare:79 | ||||
| chr6:33420059-33420301 | Rare:52; Clinvar (benign):1 | ||||
| chr6:33454436-33454588 | Rare:37 | ||||
| chr6:34236752-34236934 | Common:2; Rare:73 | ||||
| chr6:34248977-34249351 | Common:1; Rare:94 | ||||
| chr6:34425994-34426223 | Common:5; Rare:96; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696751-34696980 | Common:1; Rare:52 | ||||
| chr6:34757320-34757548 | Common:1; Rare:67 | ||||
| chr6:34887953-34888135 | Common:1; Rare:42 | ||||
| chr6:35259433-35259762 | Common:3; Rare:100 | ||||
| chr6:35921042-35921205 | Common:1; Rare:77 |