| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:12530846-12531016 | Common:2 | ||||
| chr8:12542624-12542826 | Rare:1 | ||||
| chr8:12548407-12548425 | |||||
| chr8:12549523-12549836 | Rare:4 | ||||
| chr8:12550559-12550847 | Rare:6 | ||||
| chr8:12564894-12565486 | Rare:6 | ||||
| chr8:12565627-12565895 | Common:2; Rare:23 | ||||
| chr8:12578133-12578208 | Rare:5 | ||||
| chr8:12659402-12659785 | Common:17; Rare:223 | ||||
| chr8:13110576-13110811 | Rare:71 | ||||
| chr8:13127715-13127883 | Rare:40 | ||||
| chr8:13127943-13128162 | Common:2; Rare:57 | ||||
| chr8:17793317-17793443 | Rare:32 | ||||
| chr8:17801503-17801667 | Common:4; Rare:71 | ||||
| chr8:18057460-18057858 | Common:6; Rare:126; Clinvar (benign):1; Clinvar (pathogenic):1 |