| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:68634960-68635361 | Common:2; Rare:109 | ||||
| chr6:69796579-69796649 | Common:1; Rare:15 | ||||
| chr6:69796847-69797134 | Common:1; Rare:91; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:70413222-70413585 | Common:2; Rare:102 | ||||
| chr6:70667696-70668132 | Common:5; Rare:160 | ||||
| chr6:73263146-73263279 | Common:3; Rare:37 | ||||
| chr6:73394577-73394900 | Common:4; Rare:97 | ||||
| chr6:73518331-73519239 | Common:2; Rare:271 | ||||
| chr6:73520414-73520498 | Rare:35 | ||||
| chr6:73520973-73521410 | Common:4; Rare:116 | ||||
| chr6:73521542-73521628 | Rare:24 | ||||
| chr6:73653893-73654162 | Common:3; Rare:71; Clinvar:3 | ||||
| chr6:73696019-73696220 | Common:1; Rare:41 | ||||
| chr6:75205838-75206113 | Common:1; Rare:71 | ||||
| chr6:75284587-75285085 | Common:1; Rare:164 |