| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143060690-143060935 | Common:7; Rare:89 | ||||
| chr6:143450660-143451009 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511251-143511323 | Rare:15 | ||||
| chr6:143511651-143511785 | Common:4; Rare:34 | ||||
| chr6:143607958-143608291 | Common:1; Rare:50 | ||||
| chr6:143843152-143843469 | Common:2; Rare:108 | ||||
| chr6:144150292-144150574 | Common:5; Rare:79 | ||||
| chr6:144285249-144285636 | Common:2; Rare:90 | ||||
| chr6:144286032-144286214 | Common:2; Rare:27 | ||||
| chr6:145814664-145814927 | Common:1; Rare:118 | ||||
| chr6:145815221-145815269 | Rare:9 | ||||
| chr6:145964044-145964132 | Common:4; Rare:19 | ||||
| chr6:145964306-145964616 | Rare:104 | ||||
| chr6:147204669-147204697 | Rare:7 | ||||
| chr6:148342878-148343085 | Rare:52 |