| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289774-136290041 | Common:2; Rare:116 | ||||
| chr6:137219356-137219511 | Common:4; Rare:48; Clinvar (benign):2 | ||||
| chr6:138404147-138404502 | Common:5; Rare:103 | ||||
| chr6:138773657-138773795 | Common:1; Rare:64 | ||||
| chr6:139028610-139028832 | Common:1; Rare:47 | ||||
| chr6:142147135-142147300 | Rare:64 | ||||
| chr6:142301769-142302043 | Common:5; Rare:80 | ||||
| chr6:143060724-143060919 | Common:7; Rare:67 | ||||
| chr6:143450667-143450929 | Common:1; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677828-143678032 | Common:2; Rare:49 | ||||
| chr6:144095548-144095838 | Common:5; Rare:73 | ||||
| chr6:144285171-144285498 | Common:3; Rare:87 | ||||
| chr6:145814743-145814915 | Common:1; Rare:84 | ||||
| chr6:149546003-149546149 | Rare:62 | ||||
| chr6:149718066-149718151 | Common:1; Rare:28 |