| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89145983-89146100 | Rare:35 | ||||
| chr6:89638443-89638549 | Common:1; Rare:23 | ||||
| chr6:89638713-89638845 | Common:3; Rare:47 | ||||
| chr6:89819703-89820075 | Common:1; Rare:109 | ||||
| chr6:89829602-89829962 | Rare:93 | ||||
| chr6:93419250-93419325 | Rare:23 | ||||
| chr6:93419329-93419837 | Common:1; Rare:128 | ||||
| chr6:95577368-95577593 | Common:6; Rare:62 | ||||
| chr6:96521674-96521899 | Common:8; Rare:111 | ||||
| chr6:96837469-96837649 | Common:2; Rare:53 | ||||
| chr6:96897807-96898012 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283170-97283302 | Common:1; Rare:48 | ||||
| chr6:99424668-99424963 | Rare:81 | ||||
| chr6:99425214-99425446 | Common:2; Rare:70 | ||||
| chr6:99515400-99515602 | Common:1; Rare:65 |