| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31834584-31834929 | Common:3; Rare:79 | ||||
| chr6:31897649-31897785 | Rare:28 | ||||
| chr6:31958892-31959189 | Rare:93; Clinvar:8 | ||||
| chr6:32130176-32130468 | Common:4; Rare:49 | ||||
| chr6:32154376-32154500 | Rare:15 | ||||
| chr6:32154749-32155120 | Rare:70 | ||||
| chr6:32164319-32164628 | Common:1; Rare:34 | ||||
| chr6:32176043-32176244 | Common:1; Rare:43 | ||||
| chr6:32177071-32177410 | Common:1; Rare:61 | ||||
| chr6:32178085-32178458 | Common:3; Rare:56 | ||||
| chr6:32196507-32196677 | Rare:38 | ||||
| chr6:32838680-32839125 | Common:8; Rare:70 | ||||
| chr6:32843979-32844115 | Rare:32; Clinvar:1 | ||||
| chr6:32844622-32844847 | Common:1; Rare:49 | ||||
| chr6:32853686-32853777 | Rare:42; Clinvar:2; Clinvar (benign):1 |