| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541494-42541897 | Common:3; Rare:129; Clinvar (benign):1 | ||||
| chr8:42541917-42542045 | Rare:35; Clinvar:3 | ||||
| chr8:42542129-42542217 | Rare:24; Clinvar (benign):1 | ||||
| chr8:42843277-42843477 | Common:2; Rare:54; Clinvar (benign):3 | ||||
| chr8:42896289-42896382 | Rare:38 | ||||
| chr8:42896573-42897043 | Common:1; Rare:188 | ||||
| chr8:43056105-43056463 | Common:1; Rare:127 | ||||
| chr8:43140304-43140559 | Common:2; Rare:98; Clinvar:8 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 | ||||
| chr8:47960106-47960230 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960799-47960998 | Common:1; Rare:76; Clinvar:6 | ||||
| chr8:48008220-48008456 | Common:2; Rare:112 | ||||
| chr8:51898950-51899341 | Common:8; Rare:175 | ||||
| chr8:51899607-51899670 | Rare:10 | ||||
| chr8:52714156-52714731 | Common:3; Rare:201 |