| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:68635134-68635369 | Common:1; Rare:72 | ||||
| chr6:68635715-68635958 | Rare:48 | ||||
| chr6:69796862-69797151 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:69866548-69866589 | Rare:8 | ||||
| chr6:70413222-70413577 | Common:2; Rare:98 | ||||
| chr6:70566852-70566967 | Common:1; Rare:43 | ||||
| chr6:70667696-70668025 | Common:4; Rare:126 | ||||
| chr6:73263165-73263273 | Common:2; Rare:26 | ||||
| chr6:73310136-73310268 | Common:1; Rare:37 | ||||
| chr6:73394566-73394900 | Common:5; Rare:100 | ||||
| chr6:73520973-73521406 | Common:3; Rare:113 | ||||
| chr6:73521537-73521634 | Rare:24 | ||||
| chr6:73523808-73523881 | Rare:21 | ||||
| chr6:73653915-73654176 | Common:3; Rare:71; Clinvar:3 | ||||
| chr6:73695837-73695856 | Rare:2 |