| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38030373-38030590 | Common:2; Rare:70 | ||||
| chr8:38105439-38105548 | Common:1; Rare:38 | ||||
| chr8:38176382-38176906 | Common:6; Rare:156 | ||||
| chr8:38386324-38386563 | Common:1; Rare:56 | ||||
| chr8:38406765-38406893 | Common:1; Rare:23 | ||||
| chr8:38996443-38997057 | Common:7; Rare:235 | ||||
| chr8:42271251-42271458 | Common:2; Rare:77 | ||||
| chr8:42338385-42338525 | Common:1; Rare:61 | ||||
| chr8:42391741-42391922 | Common:2; Rare:64 | ||||
| chr8:42541562-42541744 | Rare:65 | ||||
| chr8:42843290-42843523 | Common:2; Rare:66; Clinvar (benign):3 | ||||
| chr8:43056196-43056476 | Rare:110 | ||||
| chr8:47260790-47261006 | Common:3; Rare:94 | ||||
| chr8:47960106-47960240 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960775-47960997 | Common:1; Rare:84; Clinvar:7 |