| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137866935-137867233 | Rare:66 | ||||
| chr6:138107216-138107485 | Common:2; Rare:87 | ||||
| chr6:138404155-138404560 | Common:7; Rare:111 | ||||
| chr6:138572527-138572723 | Common:1; Rare:41 | ||||
| chr6:138773642-138773827 | Common:3; Rare:88 | ||||
| chr6:138988212-138988454 | Common:3; Rare:70 | ||||
| chr6:139028632-139028819 | Common:1; Rare:38 | ||||
| chr6:139029041-139029150 | Common:4; Rare:25 | ||||
| chr6:139374480-139374570 | Common:1; Rare:35 | ||||
| chr6:139374573-139374771 | Common:1; Rare:85 | ||||
| chr6:142147097-142147317 | Common:3; Rare:92 | ||||
| chr6:142301874-142302113 | Common:5; Rare:68 | ||||
| chr6:143060391-143060517 | Rare:28 | ||||
| chr6:143060697-143060944 | Common:7; Rare:85 | ||||
| chr6:143450660-143451024 | Common:1; Rare:127; Clinvar:4; Clinvar (benign):1 |