| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:35921047-35921167 | Rare:62 | ||||
| chr6:36547379-36547589 | Common:1; Rare:100 | ||||
| chr6:36594144-36594391 | Common:4; Rare:96 | ||||
| chr6:36874779-36874882 | Rare:41 | ||||
| chr6:36874965-36875172 | Common:1; Rare:35 | ||||
| chr6:38639917-38639983 | Rare:16 | ||||
| chr6:41921083-41921234 | Common:1; Rare:40 | ||||
| chr6:42879585-42879943 | Rare:102 | ||||
| chr6:42929209-42929797 | Common:6; Rare:199 | ||||
| chr6:42984284-42984629 | Rare:86 | ||||
| chr6:43013822-43014280 | Common:2; Rare:115 | ||||
| chr6:43076123-43076473 | Rare:112 | ||||
| chr6:43427644-43427880 | Rare:48 | ||||
| chr6:43477347-43477589 | Common:1; Rare:47 | ||||
| chr6:43516854-43517115 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 |