| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159762339-159762479 | Common:1; Rare:33 | ||||
| chr6:159789483-159789999 | Common:4; Rare:178 | ||||
| chr6:159790250-159790617 | Common:10; Rare:140 | ||||
| chr6:162727010-162727132 | Rare:28 | ||||
| chr6:162727701-162727985 | Rare:104; Clinvar:3 | ||||
| chr6:163415107-163415328 | Common:6; Rare:82 | ||||
| chr6:163416057-163416160 | Common:1; Rare:31 | ||||
| chr6:166342508-166342681 | Common:3; Rare:69 | ||||
| chr6:166627950-166628224 | Common:1; Rare:58 | ||||
| chr6:166956227-166956261 | Rare:5; Clinvar:1 | ||||
| chr6:166956529-166956769 | Common:5; Rare:82; Clinvar:3 | ||||
| chr6:166999092-166999415 | Common:1; Rare:110 | ||||
| chr6:167826763-167827213 | Common:2; Rare:234 | ||||
| chr6:169702004-169702201 | Common:3; Rare:101 | ||||
| chr6:169751534-169751644 | Rare:39; Clinvar (benign):1 |