| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:134942438-134942767 | Rare:77 | ||||
| chr6:137723988-137724118 | Rare:25 | ||||
| chr6:137724128-137724256 | Rare:26 | ||||
| chr6:137868212-137868236 | Rare:2 | ||||
| chr6:139027835-139028112 | Common:1; Rare:47 | ||||
| chr6:147510001-147510156 | Common:2; Rare:31 | ||||
| chr6:159716329-159716516 | Common:2; Rare:31 | ||||
| chr6:160100798-160100817 | Rare:1 | ||||
| chr6:160520281-160520586 | Common:5; Rare:98 | ||||
| chr6:160708993-160709016 | Rare:2 | ||||
| chr6:160718265-160718835 | Common:3; Rare:149; Clinvar (pathogenic):1 | ||||
| chr6:167791188-167791307 | Common:1; Rare:13 | ||||
| chr6:168197013-168197219 | Common:4; Rare:43 | ||||
| chr6:169702768-169703021 | Common:2; Rare:107 | ||||
| chr6:169704773-169704905 | Rare:33 |