| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46652748-46652991 | Rare:66 | ||||
| chr6:49463148-49463438 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52419984-52420411 | Common:3; Rare:167; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:52576766-52577307 | Common:8; Rare:193 | ||||
| chr6:52577333-52577444 | Common:1; Rare:38 | ||||
| chr6:52995266-52995615 | Common:4; Rare:136 | ||||
| chr6:53092162-53092474 | Common:1; Rare:61 | ||||
| chr6:53348922-53349260 | Common:2; Rare:108 | ||||
| chr6:53545099-53545332 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr6:56462474-56462711 | Rare:42 | ||||
| chr6:56482077-56482417 | Common:2; Rare:77 | ||||
| chr6:56542782-56543014 | Common:2; Rare:41 | ||||
| chr6:56843086-56843105 | Rare:2 | ||||
| chr6:56843571-56843935 | Common:9; Rare:86 | ||||
| chr6:56851558-56851638 | Rare:26 |