| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131063148-131063468 | Rare:94 | ||||
| chr6:132401428-132401568 | Common:1; Rare:44 | ||||
| chr6:132814255-132814612 | Common:4; Rare:130 | ||||
| chr6:133953058-133953291 | Common:2; Rare:78 | ||||
| chr6:134174857-134175059 | Common:1; Rare:95 | ||||
| chr6:134175685-134175966 | Common:2; Rare:65 | ||||
| chr6:134177843-134177967 | Rare:21 | ||||
| chr6:135054785-135054950 | Common:6; Rare:51 | ||||
| chr6:135497604-135497880 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289768-136290024 | Common:1; Rare:111 | ||||
| chr6:136584526-136584680 | Common:1; Rare:23 | ||||
| chr6:138773646-138773827 | Common:3; Rare:86 | ||||
| chr6:142147130-142147290 | Common:1; Rare:58 | ||||
| chr6:142301822-142302154 | Common:6; Rare:97 | ||||
| chr6:143060742-143060919 | Common:7; Rare:61 |