| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:70566792-70566993 | Common:2; Rare:74 | ||||
| chr6:71288297-71288466 | Common:2; Rare:33 | ||||
| chr6:72621315-72621641 | Common:2; Rare:85 | ||||
| chr6:72622068-72622476 | Common:4; Rare:102 | ||||
| chr6:73263153-73263279 | Common:3; Rare:34 | ||||
| chr6:73310144-73310198 | Common:1; Rare:14 | ||||
| chr6:73394597-73394908 | Common:4; Rare:99 | ||||
| chr6:73451871-73451939 | Common:1; Rare:26; Clinvar:1 | ||||
| chr6:73452274-73452361 | Common:1; Rare:15 | ||||
| chr6:73519868-73520499 | Common:2; Rare:232 | ||||
| chr6:73520988-73521411 | Common:4; Rare:112 | ||||
| chr6:73521545-73521647 | Rare:30 | ||||
| chr6:73521810-73521861 | Rare:14 | ||||
| chr6:73523793-73523871 | Rare:23 | ||||
| chr6:73653816-73654176 | Common:3; Rare:105; Clinvar:3; Clinvar (pathogenic):1 |