| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289773-136290014 | Common:1; Rare:104 | ||||
| chr6:136525695-136525837 | Common:1; Rare:24 | ||||
| chr6:136526032-136526249 | Rare:33 | ||||
| chr6:136526251-136526650 | Common:8; Rare:78 | ||||
| chr6:136550346-136550701 | Common:2; Rare:107 | ||||
| chr6:137219323-137219473 | Common:2; Rare:54; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138107410-138107607 | Common:5; Rare:49 | ||||
| chr6:138773702-138773855 | Common:3; Rare:73 | ||||
| chr6:142147129-142147366 | Common:1; Rare:99 | ||||
| chr6:142301816-142302123 | Common:8; Rare:88 | ||||
| chr6:142302494-142302730 | Common:1; Rare:49 | ||||
| chr6:143060735-143061061 | Common:8; Rare:114 | ||||
| chr6:143450579-143450996 | Common:1; Rare:144; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511649-143511795 | Common:4; Rare:36 | ||||
| chr6:143843288-143843478 | Common:1; Rare:67 |