| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118548163-118548390 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:118651501-118651737 | Common:3; Rare:74 | ||||
| chr6:118893819-118894313 | Common:10; Rare:145 | ||||
| chr6:118934978-118935061 | Common:3; Rare:24 | ||||
| chr6:119349626-119349935 | Common:4; Rare:103 | ||||
| chr6:121334472-121334779 | Common:6; Rare:78 | ||||
| chr6:122471733-122471923 | Common:2; Rare:60 | ||||
| chr6:122789467-122789788 | Common:2; Rare:90 | ||||
| chr6:124963016-124963219 | Common:1; Rare:75 | ||||
| chr6:124963523-124963697 | Rare:31 | ||||
| chr6:125749413-125749784 | Common:5; Rare:146 | ||||
| chr6:125781059-125781156 | Rare:18 | ||||
| chr6:125986375-125986673 | Rare:114 | ||||
| chr6:126340056-126340250 | Rare:65 | ||||
| chr6:127118966-127119151 | Rare:39 |