| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145814780-145814927 | Common:1; Rare:71 | ||||
| chr6:145964327-145964531 | Rare:66 | ||||
| chr6:149718089-149718285 | Common:3; Rare:57 | ||||
| chr6:149941866-149942033 | Common:4; Rare:29 | ||||
| chr6:150599320-150599503 | Common:1; Rare:35 | ||||
| chr6:150599805-150599996 | Rare:73 | ||||
| chr6:151391529-151391887 | Common:3; Rare:99 | ||||
| chr6:151452117-151452542 | Common:3; Rare:144 | ||||
| chr6:153002666-153002870 | Common:4; Rare:68 | ||||
| chr6:158168259-158168392 | Common:2; Rare:49 | ||||
| chr6:158644713-158644943 | Common:2; Rare:83 | ||||
| chr6:158819333-158819535 | Common:2; Rare:75 | ||||
| chr6:158999765-158999975 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:159044908-159045153 | Common:1; Rare:48 | ||||
| chr6:159693253-159693637 | Common:5; Rare:119 |