Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:41577985-41578256 | Rare:85 | ||||
chr8:42051974-42052263 | Common:1; Rare:85 | ||||
chr8:42541118-42541178 | Rare:11 | ||||
chr8:42541559-42541661 | Rare:34 | ||||
chr8:42541680-42541977 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
chr8:42843031-42843092 | Rare:17; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr8:42843273-42843461 | Common:2; Rare:47; Clinvar (benign):3 | ||||
chr8:42896683-42897027 | Common:1; Rare:140 | ||||
chr8:43056163-43056463 | Common:1; Rare:115 | ||||
chr8:47260790-47260981 | Common:3; Rare:82 | ||||
chr8:47960090-47960193 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
chr8:47960799-47960990 | Common:1; Rare:71; Clinvar:6 | ||||
chr8:48008348-48008456 | Common:2; Rare:67 | ||||
chr8:51898984-51899334 | Common:7; Rare:156 | ||||
chr8:52714377-52714603 | Common:1; Rare:101 |