| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132881737-132882099 | Common:1; Rare:82; Clinvar:1 | ||||
| chr8:133250420-133250644 | Rare:65; Clinvar:5; Clinvar (benign):1 | ||||
| chr8:133571821-133572185 | Rare:89 | ||||
| chr8:134713008-134713149 | Common:1; Rare:45 | ||||
| chr8:140457678-140457884 | Common:4; Rare:62 | ||||
| chr8:140511252-140511646 | Common:2; Rare:144 | ||||
| chr8:141001136-141001428 | Common:2; Rare:96 | ||||
| chr8:142669940-142670328 | Common:9; Rare:134 | ||||
| chr8:142700408-142700536 | Common:3; Rare:59 | ||||
| chr8:142741808-142742043 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr8:142742328-142742448 | Common:2; Rare:38; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:142769754-142769908 | Rare:61 | ||||
| chr8:142785847-142785873 | Rare:4 | ||||
| chr8:142786095-142786119 | Rare:5 | ||||
| chr8:142786463-142786617 | Common:4; Rare:36 |