| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149749647-149749816 | Rare:92 | ||||
| chr6:149941869-149942026 | Common:4; Rare:28 | ||||
| chr6:150069056-150069172 | Common:2; Rare:27 | ||||
| chr6:150368781-150369206 | Rare:103; Clinvar:4 | ||||
| chr6:150369725-150370072 | Common:1; Rare:73 | ||||
| chr6:150370363-150370658 | Common:2; Rare:66 | ||||
| chr6:150599796-150599974 | Common:1; Rare:69 | ||||
| chr6:151240218-151240434 | Common:2; Rare:56 | ||||
| chr6:151325409-151325727 | Common:2; Rare:72 | ||||
| chr6:151325828-151325884 | Rare:18 | ||||
| chr6:151390943-151391104 | Common:1; Rare:48 | ||||
| chr6:151391495-151391849 | Common:3; Rare:103 | ||||
| chr6:151452019-151452552 | Common:5; Rare:190; Clinvar (benign):3 | ||||
| chr6:151452569-151452749 | Common:1; Rare:43 | ||||
| chr6:152301888-152302217 | Common:1; Rare:110; Clinvar:9; Clinvar (benign):5 |