| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30720117-30720551 | Common:1; Rare:99 | ||||
| chr6:30721374-30721668 | Rare:137 | ||||
| chr6:30742457-30742974 | Common:3; Rare:120 | ||||
| chr6:30886514-30886659 | Rare:23 | ||||
| chr6:30914190-30914402 | Rare:75; Clinvar (benign):2 | ||||
| chr6:31158160-31158643 | Common:9; Rare:116 | ||||
| chr6:31541938-31542425 | Common:8; Rare:139 | ||||
| chr6:31546555-31546893 | Common:3; Rare:66 | ||||
| chr6:31547415-31547731 | Common:2; Rare:80 | ||||
| chr6:31615329-31615581 | Common:4; Rare:47 | ||||
| chr6:31620321-31620818 | Common:1; Rare:155 | ||||
| chr6:31652326-31652463 | Common:7; Rare:46 | ||||
| chr6:31652601-31652759 | Common:2; Rare:35 | ||||
| chr6:31660676-31660868 | Rare:57 | ||||
| chr6:31664902-31665459 | Common:5; Rare:143 |