| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31739685-31740032 | Common:3; Rare:90 | ||||
| chr6:31815278-31815546 | Common:1; Rare:80 | ||||
| chr6:31834618-31834924 | Common:3; Rare:69 | ||||
| chr6:31897654-31897782 | Rare:25 | ||||
| chr6:31958891-31959198 | Rare:102; Clinvar:8 | ||||
| chr6:32128188-32128460 | Common:2; Rare:73 | ||||
| chr6:32130179-32130399 | Common:2; Rare:40 | ||||
| chr6:32190146-32190395 | Rare:46 | ||||
| chr6:32838212-32838362 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr6:32838710-32839125 | Common:7; Rare:65 | ||||
| chr6:32843992-32844119 | Rare:29; Clinvar:1 | ||||
| chr6:32844305-32844840 | Common:1; Rare:117 | ||||
| chr6:32853670-32853778 | Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32853989-32854209 | Common:2; Rare:51 | ||||
| chr6:33200639-33201025 | Common:3; Rare:102 |