| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:70566852-70566975 | Common:1; Rare:49 | ||||
| chr6:70667704-70668101 | Common:5; Rare:148 | ||||
| chr6:73263135-73263286 | Common:4; Rare:42 | ||||
| chr6:73369628-73369712 | Common:1; Rare:33 | ||||
| chr6:73369851-73369943 | Rare:27 | ||||
| chr6:73394597-73394932 | Common:5; Rare:114 | ||||
| chr6:73462039-73462111 | Rare:20; Clinvar (benign):1 | ||||
| chr6:73518346-73519230 | Common:1; Rare:263 | ||||
| chr6:73520174-73520523 | Common:1; Rare:135 | ||||
| chr6:73520525-73520603 | Rare:26 | ||||
| chr6:73520938-73521202 | Common:3; Rare:82 | ||||
| chr6:73521204-73521303 | Rare:23 | ||||
| chr6:73521542-73521706 | Rare:45 | ||||
| chr6:73523816-73523857 | Rare:13 | ||||
| chr6:73653956-73654183 | Common:3; Rare:64; Clinvar:2 |