| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149546010-149546166 | Common:1; Rare:66 | ||||
| chr6:149718070-149718142 | Common:1; Rare:22 | ||||
| chr6:149749523-149749783 | Rare:115 | ||||
| chr6:151452035-151452352 | Common:3; Rare:105 | ||||
| chr6:152983021-152983281 | Common:2; Rare:78 | ||||
| chr6:157323506-157323597 | Common:2; Rare:29 | ||||
| chr6:158168230-158168382 | Common:2; Rare:52 | ||||
| chr6:159726926-159727162 | Common:1; Rare:91 | ||||
| chr6:159761822-159762077 | Common:4; Rare:126 | ||||
| chr6:159789553-159789993 | Common:4; Rare:150 | ||||
| chr6:166342524-166342638 | Common:2; Rare:43 | ||||
| chr6:166999050-166999402 | Common:1; Rare:119 | ||||
| chr6:169751526-169751643 | Rare:40; Clinvar (benign):1 | ||||
| chr7:727249-727304 | Rare:15; Clinvar:1 | ||||
| chr7:1138233-1138471 | Common:2; Rare:73 |