| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137870808-137871166 | Common:2; Rare:72 | ||||
| chr6:138107400-138107614 | Common:5; Rare:56 | ||||
| chr6:138773646-138773854 | Common:3; Rare:92 | ||||
| chr6:138795912-138796097 | Common:1; Rare:43 | ||||
| chr6:139028628-139028832 | Common:1; Rare:42 | ||||
| chr6:142147128-142147287 | Common:1; Rare:56 | ||||
| chr6:142301722-142302107 | Common:8; Rare:107 | ||||
| chr6:142945178-142945473 | Common:1; Rare:68 | ||||
| chr6:143060723-143060935 | Common:7; Rare:77 | ||||
| chr6:143450660-143450915 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843151-143843454 | Common:2; Rare:100 | ||||
| chr6:145814669-145814943 | Common:1; Rare:125 | ||||
| chr6:145964035-145964187 | Common:4; Rare:35 | ||||
| chr6:147204568-147204652 | Rare:25 | ||||
| chr6:149546001-149546173 | Common:1; Rare:75 |