| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:117999195-117999242 | Common:1; Rare:9 | ||||
| chr6:119350582-119350722 | Common:2; Rare:29 | ||||
| chr6:121437161-121437314 | Common:3; Rare:30 | ||||
| chr6:121437479-121437656 | Common:1; Rare:41 | ||||
| chr6:121438510-121438635 | Rare:31 | ||||
| chr6:127117408-127117655 | Common:1; Rare:44 | ||||
| chr6:127120781-127121004 | Rare:45 | ||||
| chr6:129453931-129454310 | Common:2; Rare:91; Clinvar:5; Clinvar (benign):5 | ||||
| chr6:129459950-129460320 | Common:2; Rare:89; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr6:129481036-129481287 | Common:1; Rare:46; Clinvar (benign):2 | ||||
| chr6:129486226-129486568 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129505005-129505333 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129512277-129512485 | Rare:64; Clinvar:5; Clinvar (benign):2 | ||||
| chr6:134437527-134437720 | Common:1; Rare:24 | ||||
| chr6:134905645-134905682 | Rare:9 |