| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138773345-138773621 | Common:2; Rare:111 | ||||
| chr6:138773646-138773865 | Common:3; Rare:97 | ||||
| chr6:139028597-139028858 | Common:1; Rare:55 | ||||
| chr6:142147140-142147287 | Rare:54 | ||||
| chr6:142301848-142302173 | Common:6; Rare:93 | ||||
| chr6:143060724-143060919 | Common:7; Rare:67 | ||||
| chr6:143450654-143450956 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843201-143843428 | Common:2; Rare:72 | ||||
| chr6:144150304-144150529 | Common:5; Rare:62 | ||||
| chr6:144285242-144285510 | Common:2; Rare:60 | ||||
| chr6:144286183-144286358 | Common:1; Rare:38 | ||||
| chr6:145814718-145814898 | Common:1; Rare:87 | ||||
| chr6:148342340-148342441 | Rare:19 | ||||
| chr6:148342912-148343178 | Common:1; Rare:96 | ||||
| chr6:149546010-149546155 | Rare:61 |