| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7108553-7108685 | Common:1; Rare:45 | ||||
| chr6:7313042-7313380 | Common:5; Rare:126 | ||||
| chr6:7389341-7389490 | Rare:28 | ||||
| chr6:7389504-7389974 | Common:3; Rare:123 | ||||
| chr6:7541334-7541553 | Common:2; Rare:73 | ||||
| chr6:7541560-7542085 | Common:4; Rare:172; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr6:7910633-7910914 | Common:3; Rare:109 | ||||
| chr6:8064321-8064576 | Common:4; Rare:85 | ||||
| chr6:8435440-8435689 | Common:5; Rare:90 | ||||
| chr6:10412342-10412612 | Common:3; Rare:50 | ||||
| chr6:10412977-10413095 | Rare:32 | ||||
| chr6:10415029-10415190 | Common:1; Rare:53 | ||||
| chr6:10415263-10415412 | Rare:34 | ||||
| chr6:10419542-10419680 | Rare:29 | ||||
| chr6:10521195-10521526 | Common:1; Rare:80 |