| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159693218-159693579 | Common:6; Rare:101 | ||||
| chr6:159726911-159727029 | Common:1; Rare:52 | ||||
| chr6:159727044-159727234 | Rare:59 | ||||
| chr6:159727330-159727625 | Common:5; Rare:126 | ||||
| chr6:159761758-159762067 | Common:6; Rare:141 | ||||
| chr6:159762339-159762479 | Common:1; Rare:33 | ||||
| chr6:159789538-159790005 | Common:4; Rare:155 | ||||
| chr6:159790244-159790514 | Common:7; Rare:86 | ||||
| chr6:160991476-160991792 | Common:5; Rare:89 | ||||
| chr6:162726949-162727199 | Common:4; Rare:57 | ||||
| chr6:162727633-162728081 | Common:3; Rare:166; Clinvar:7; Clinvar (pathogenic):2 | ||||
| chr6:163413430-163413696 | Common:3; Rare:75 | ||||
| chr6:163415102-163415328 | Common:6; Rare:83 | ||||
| chr6:163416006-163416253 | Common:2; Rare:61 | ||||
| chr6:166342496-166342665 | Common:3; Rare:67 |