| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30651125-30651369 | Common:1; Rare:47 | ||||
| chr6:30672640-30672742 | Common:1; Rare:44 | ||||
| chr6:30672905-30673207 | Common:3; Rare:97 | ||||
| chr6:30717257-30717435 | Common:1; Rare:37 | ||||
| chr6:30720124-30720409 | Common:1; Rare:73 | ||||
| chr6:30742616-30742961 | Common:2; Rare:82 | ||||
| chr6:30744535-30744778 | Common:2; Rare:52 | ||||
| chr6:30914160-30914396 | Rare:79; Clinvar (benign):2 | ||||
| chr6:31158165-31158504 | Common:8; Rare:79 | ||||
| chr6:31269337-31269514 | Common:9; Rare:50 | ||||
| chr6:31269964-31270493 | Common:60; Rare:167 | ||||
| chr6:31271927-31272231 | Common:21; Rare:70 | ||||
| chr6:31355105-31355469 | Common:20; Rare:117 | ||||
| chr6:31357068-31357339 | Common:28; Rare:61 | ||||
| chr6:31541953-31542387 | Common:8; Rare:122 |