| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30717257-30717672 | Common:3; Rare:91 | ||||
| chr6:30720128-30720563 | Common:1; Rare:97 | ||||
| chr6:30721293-30721692 | Common:2; Rare:165 | ||||
| chr6:30742616-30742979 | Common:2; Rare:87 | ||||
| chr6:30880674-30881027 | Common:1; Rare:68 | ||||
| chr6:30886473-30886527 | Rare:10 | ||||
| chr6:30914209-30914344 | Rare:56; Clinvar (benign):1 | ||||
| chr6:31158165-31158620 | Common:8; Rare:113 | ||||
| chr6:31197998-31198039 | Rare:8 | ||||
| chr6:31272034-31272238 | Common:13; Rare:41 | ||||
| chr6:31541915-31542338 | Common:8; Rare:109 | ||||
| chr6:31546477-31546916 | Common:3; Rare:86 | ||||
| chr6:31547409-31547728 | Common:2; Rare:81 | ||||
| chr6:31620321-31620857 | Common:1; Rare:166 | ||||
| chr6:31625800-31626157 | Rare:110 |