| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30740495-30740814 | Common:1; Rare:74 | ||||
| chr6:30742466-30742965 | Common:3; Rare:115 | ||||
| chr6:30911965-30912456 | Common:6; Rare:125 | ||||
| chr6:30914079-30914353 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr6:31158159-31158628 | Common:8; Rare:115 | ||||
| chr6:31399742-31399786 | Rare:11 | ||||
| chr6:31399956-31400088 | Common:4; Rare:33 | ||||
| chr6:31540704-31540845 | Common:1; Rare:30 | ||||
| chr6:31541911-31542320 | Common:7; Rare:109 | ||||
| chr6:31542401-31542542 | Rare:45 | ||||
| chr6:31546553-31546957 | Common:3; Rare:79 | ||||
| chr6:31547428-31547728 | Common:2; Rare:79 | ||||
| chr6:31620348-31620853 | Common:1; Rare:157 | ||||
| chr6:31636209-31636603 | Common:4; Rare:130 | ||||
| chr6:31640383-31640677 | Rare:72 |