| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537336-79537658 | Common:2; Rare:99; Clinvar:4 | ||||
| chr6:79947531-79947810 | Common:1; Rare:103; Clinvar:6; Clinvar (benign):1 | ||||
| chr6:80004355-80004697 | Common:7; Rare:84 | ||||
| chr6:81752642-81752854 | Rare:112 | ||||
| chr6:82247677-82248020 | Common:1; Rare:108 | ||||
| chr6:83067443-83067748 | Common:1; Rare:76 | ||||
| chr6:83193183-83193397 | Common:3; Rare:71 | ||||
| chr6:85449521-85449749 | Common:2; Rare:58 | ||||
| chr6:85449954-85450267 | Common:1; Rare:91 | ||||
| chr6:85593706-85594107 | Common:2; Rare:123 | ||||
| chr6:85643812-85643918 | Common:2; Rare:34 | ||||
| chr6:85644159-85644264 | Rare:20 | ||||
| chr6:87155242-87155594 | Rare:93 | ||||
| chr6:87589955-87590171 | Common:3; Rare:99; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702221-87702517 | Common:1; Rare:92 |