| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138988274-138988303 | Rare:8 | ||||
| chr6:139028401-139028543 | Common:1; Rare:22 | ||||
| chr6:139028629-139028912 | Common:1; Rare:61 | ||||
| chr6:139029041-139029146 | Common:4; Rare:24 | ||||
| chr6:139374469-139374809 | Common:2; Rare:139 | ||||
| chr6:142147128-142147290 | Common:1; Rare:58 | ||||
| chr6:142301833-142302212 | Common:6; Rare:107 | ||||
| chr6:142302463-142302696 | Common:1; Rare:45 | ||||
| chr6:143060742-143060928 | Common:7; Rare:66 | ||||
| chr6:143450579-143450941 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511651-143511790 | Common:4; Rare:35 | ||||
| chr6:143843152-143843415 | Common:2; Rare:83 | ||||
| chr6:144095501-144095749 | Common:5; Rare:87 | ||||
| chr6:144150331-144150517 | Common:5; Rare:53 | ||||
| chr6:144285182-144285372 | Common:3; Rare:55 |