| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32838695-32838979 | Common:6; Rare:45 | ||||
| chr6:32843851-32844271 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32844327-32844860 | Common:1; Rare:116 | ||||
| chr6:32853646-32853923 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32854019-32854250 | Common:2; Rare:58 | ||||
| chr6:32952948-32952955 | |||||
| chr6:32952959-32953115 | Rare:36 | ||||
| chr6:32968461-32968652 | Common:2; Rare:59 | ||||
| chr6:33009525-33009826 | Common:4; Rare:67 | ||||
| chr6:33075901-33076112 | Common:3; Rare:38 | ||||
| chr6:33200654-33200935 | Common:2; Rare:84 | ||||
| chr6:33271836-33272125 | Common:1; Rare:118 | ||||
| chr6:33288988-33289096 | Rare:41 | ||||
| chr6:33289175-33289325 | Common:1; Rare:46 | ||||
| chr6:33298900-33299066 | Rare:43 |