| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123540907-123541368 | Common:4; Rare:147 | ||||
| chr8:123768318-123768633 | Common:5; Rare:100 | ||||
| chr8:124474516-124474778 | Common:1; Rare:95 | ||||
| chr8:124474963-124475099 | Rare:44 | ||||
| chr8:124539026-124539189 | Common:2; Rare:92; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124546968-124547038 | Rare:17 | ||||
| chr8:124556281-124556519 | Common:1; Rare:66 | ||||
| chr8:124673305-124673678 | Common:2; Rare:72 | ||||
| chr8:124727882-124728211 | Common:1; Rare:71 | ||||
| chr8:124728393-124728608 | Rare:61 | ||||
| chr8:125091702-125091900 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558279-126558628 | Common:1; Rare:122 | ||||
| chr8:127735294-127735617 | Rare:55 | ||||
| chr8:127735846-127736374 | Common:3; Rare:128 | ||||
| chr8:132675529-132675652 | Rare:35 |