| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132965906-132965991 | Rare:9 | ||||
| chr8:132966445-132966771 | Common:6; Rare:83; Clinvar (benign):1 | ||||
| chr8:132967074-132967340 | Common:12; Rare:52 | ||||
| chr8:132967742-132968076 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:132974843-132975046 | Common:1; Rare:32 | ||||
| chr8:132981015-132981688 | Common:3; Rare:128 | ||||
| chr8:132981691-132982339 | Common:5; Rare:132 | ||||
| chr8:132983737-132983934 | Common:1; Rare:34 | ||||
| chr8:132984627-132984938 | Rare:45 | ||||
| chr8:132987688-132988349 | Common:6; Rare:140 | ||||
| chr8:132990774-132991390 | Common:6; Rare:118 | ||||
| chr8:132992906-132993343 | Common:4; Rare:65 | ||||
| chr8:132994011-132994267 | Rare:41 | ||||
| chr8:132994562-132995500 | Common:6; Rare:177 | ||||
| chr8:132995507-132996049 | Common:1; Rare:99 |