| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142147079-142147290 | Common:3; Rare:77 | ||||
| chr6:143060724-143060926 | Common:7; Rare:71 | ||||
| chr6:143450666-143450921 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677811-143678094 | Common:2; Rare:70 | ||||
| chr6:143806432-143806599 | Common:1; Rare:36 | ||||
| chr6:143843152-143843430 | Common:2; Rare:89 | ||||
| chr6:145814715-145814921 | Common:1; Rare:97 | ||||
| chr6:148272094-148272376 | Rare:54 | ||||
| chr6:149546001-149546141 | Rare:58 | ||||
| chr6:149718069-149718153 | Common:1; Rare:28 | ||||
| chr6:149749518-149749796 | Rare:122 | ||||
| chr6:149941774-149942036 | Common:7; Rare:44 | ||||
| chr6:150720889-150721151 | Common:2; Rare:51 | ||||
| chr6:150865646-150865964 | Common:3; Rare:78 | ||||
| chr6:150866360-150866512 | Rare:61 |