| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118589199-118589327 | Rare:27 | ||||
| chr6:129395274-129395462 | Common:2; Rare:48 | ||||
| chr6:129399559-129399586 | Rare:4 | ||||
| chr6:129481023-129481439 | Common:1; Rare:101; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr6:129491685-129492025 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:129505058-129505322 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129514085-129514519 | Common:1; Rare:115; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:131949644-131950203 | Common:1; Rare:140 | ||||
| chr6:131950265-131950705 | Common:3; Rare:129 | ||||
| chr6:136288806-136289062 | Common:1; Rare:55 | ||||
| chr6:136785271-136785537 | Common:1; Rare:46 | ||||
| chr6:142946250-142946307 | Rare:17 | ||||
| chr6:148532626-148532839 | Common:3; Rare:51 | ||||
| chr6:150683353-150683620 | Common:1; Rare:49 | ||||
| chr6:169162955-169163270 | Common:3; Rare:68 |