| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120811045-120811223 | Common:3; Rare:58 | ||||
| chr8:120812133-120812184 | Rare:8 | ||||
| chr8:120812450-120812731 | Rare:52 | ||||
| chr8:122781107-122781306 | Common:1; Rare:39 | ||||
| chr8:122781589-122781932 | Common:3; Rare:66 | ||||
| chr8:123416336-123416846 | Common:1; Rare:130 | ||||
| chr8:124372672-124372839 | Common:1; Rare:59 | ||||
| chr8:124474532-124474767 | Rare:88 | ||||
| chr8:124474946-124475243 | Rare:106 | ||||
| chr8:124538981-124539287 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124546765-124547056 | Rare:63; Clinvar (pathogenic):1 | ||||
| chr8:124728213-124728267 | Common:1; Rare:6 | ||||
| chr8:124728396-124728652 | Common:2; Rare:79 | ||||
| chr8:125091617-125091934 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:125430014-125430317 | Common:1; Rare:66 |