| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138773646-138773846 | Common:3; Rare:90 | ||||
| chr6:139028606-139028832 | Common:1; Rare:48 | ||||
| chr6:142147140-142147294 | Rare:58 | ||||
| chr6:142301874-142302166 | Common:5; Rare:87 | ||||
| chr6:143060724-143060919 | Common:7; Rare:67 | ||||
| chr6:143450597-143450936 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511660-143511855 | Common:4; Rare:45 | ||||
| chr6:143843179-143843452 | Common:2; Rare:90 | ||||
| chr6:144285242-144285517 | Common:2; Rare:62 | ||||
| chr6:145814669-145814915 | Common:1; Rare:111 | ||||
| chr6:145964245-145964549 | Common:1; Rare:99 | ||||
| chr6:148342940-148343221 | Common:1; Rare:106 | ||||
| chr6:149546010-149546159 | Rare:63 | ||||
| chr6:149749545-149749796 | Rare:115 | ||||
| chr6:151240158-151240437 | Common:2; Rare:73 |