| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144413542-144413733 | Common:1; Rare:60; Clinvar:1 | ||||
| chr8:144427719-144427975 | Common:1; Rare:70 | ||||
| chr8:144428455-144428644 | Common:2; Rare:72 | ||||
| chr8:144444364-144444790 | Common:1; Rare:129 | ||||
| chr8:144462861-144463095 | Rare:115 | ||||
| chr8:144465334-144465553 | Common:3; Rare:78 | ||||
| chr8:144466842-144466954 | Common:3; Rare:60 | ||||
| chr8:144470476-144470552 | Rare:17 | ||||
| chr8:144477871-144478132 | Common:7; Rare:92 | ||||
| chr8:144504437-144504549 | Rare:39 | ||||
| chr8:144508954-144509099 | Rare:38 | ||||
| chr8:144517689-144518029 | Common:1; Rare:116; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144528912-144529168 | Common:2; Rare:108 | ||||
| chr8:144755421-144755625 | Rare:82 | ||||
| chr8:144787262-144787370 | Rare:31 |