Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10474814-10474984 | Rare:57; Clinvar:1 | ||||
chr1:11099779-11099997 | Common:2; Rare:88 | ||||
chr1:11262469-11262836 | Common:2; Rare:109 | ||||
chr1:11654396-11654505 | Rare:31 | ||||
chr1:11654811-11654931 | Common:2; Rare:34 | ||||
chr1:11805876-11806265 | Common:2; Rare:110; Clinvar:2 | ||||
chr1:11934650-11934770 | Common:1; Rare:46; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980124-11980473 | Common:6; Rare:118; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12617190-12617322 | Rare:40 | ||||
chr1:12618134-12618475 | Common:3; Rare:69 | ||||
chr1:13700164-13700277 | Rare:45 | ||||
chr1:13749154-13749477 | Common:2; Rare:119 | ||||
chr1:14929529-14929870 | Common:6; Rare:67 | ||||
chr1:15152467-15152820 | Common:6; Rare:61 | ||||
chr1:15153595-15153769 | Common:1; Rare:44 |