| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:63635629-63635896 | Rare:105 | ||||
| chr6:68634970-68635357 | Common:2; Rare:107 | ||||
| chr6:69796862-69797179 | Common:1; Rare:96; Clinvar:6; Clinvar (benign):3 | ||||
| chr6:70413156-70413573 | Common:2; Rare:129 | ||||
| chr6:70566795-70566997 | Common:2; Rare:74 | ||||
| chr6:70667702-70668135 | Common:5; Rare:159 | ||||
| chr6:73263144-73263325 | Common:5; Rare:49 | ||||
| chr6:73310144-73310275 | Common:1; Rare:34 | ||||
| chr6:73310344-73310503 | Common:2; Rare:41 | ||||
| chr6:73451841-73452023 | Common:2; Rare:66; Clinvar:1 | ||||
| chr6:73452229-73452411 | Common:1; Rare:28 | ||||
| chr6:73461700-73461814 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr6:73519517-73519802 | Common:3; Rare:102 | ||||
| chr6:73520076-73520533 | Common:1; Rare:173 | ||||
| chr6:73520956-73521410 | Common:4; Rare:120 |