| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31827390-31827746 | Common:4; Rare:179 | ||||
| chr6:31834512-31835157 | Common:13; Rare:363 | ||||
| chr6:31862780-31863140 | Common:6; Rare:177; Clinvar:5; Clinvar (benign):2 | ||||
| chr6:31897646-31897814 | Rare:65 | ||||
| chr6:31902156-31902442 | Common:4; Rare:159 | ||||
| chr6:31945824-31946193 | Common:2; Rare:84; Clinvar (benign):2 | ||||
| chr6:31958829-31959394 | Rare:281; Clinvar:16 | ||||
| chr6:32046614-32046722 | Common:1; Rare:16 | ||||
| chr6:32046940-32047400 | Common:3; Rare:178 | ||||
| chr6:32128151-32128433 | Common:4; Rare:128 | ||||
| chr6:32130158-32130462 | Common:4; Rare:49 | ||||
| chr6:32153095-32153678 | Rare:144 | ||||
| chr6:32153746-32154250 | Common:8; Rare:165 | ||||
| chr6:32154318-32154513 | Rare:47 | ||||
| chr6:32154560-32155030 | Common:4; Rare:197 |