| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79078135-79078633 | Common:1; Rare:203 | ||||
| chr6:79537373-79537579 | Common:1; Rare:56; Clinvar:3 | ||||
| chr6:79947469-79947811 | Common:2; Rare:118; Clinvar:8; Clinvar (benign):2 | ||||
| chr6:80004477-80004720 | Common:4; Rare:58 | ||||
| chr6:80106401-80106715 | Common:2; Rare:111; Clinvar (pathogenic):1 | ||||
| chr6:81752652-81752853 | Rare:105 | ||||
| chr6:82247693-82248002 | Common:1; Rare:103 | ||||
| chr6:83065733-83065935 | Common:1; Rare:71 | ||||
| chr6:83193192-83193414 | Common:3; Rare:75 | ||||
| chr6:83430894-83431249 | Common:5; Rare:119 | ||||
| chr6:84763446-84763636 | Rare:47 | ||||
| chr6:84764572-84764865 | Common:1; Rare:88 | ||||
| chr6:85449932-85450150 | Common:1; Rare:66 | ||||
| chr6:85593714-85593919 | Common:1; Rare:73 | ||||
| chr6:85642800-85643080 | Common:3; Rare:97 |