| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537340-79537676 | Common:2; Rare:107; Clinvar:4 | ||||
| chr6:80004359-80004689 | Common:7; Rare:82 | ||||
| chr6:81752648-81752851 | Rare:108 | ||||
| chr6:82247704-82247894 | Common:1; Rare:66 | ||||
| chr6:83193210-83193403 | Common:3; Rare:68 | ||||
| chr6:83431049-83431175 | Common:3; Rare:41 | ||||
| chr6:85593714-85594027 | Common:1; Rare:102 | ||||
| chr6:85642824-85643071 | Common:3; Rare:88 | ||||
| chr6:85643784-85643931 | Common:3; Rare:45 | ||||
| chr6:87155240-87155629 | Rare:112 | ||||
| chr6:87472892-87473004 | Common:1; Rare:42; Clinvar (benign):4 | ||||
| chr6:87589953-87590169 | Common:3; Rare:98; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701813-87701959 | Common:1; Rare:48 | ||||
| chr6:87702214-87702526 | Common:1; Rare:96 | ||||
| chr6:88963531-88963830 | Common:2; Rare:97 |