Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816912-42817212 | Common:1; Rare:83 | ||||
chr1:42817270-42817518 | Rare:80 | ||||
chr1:42846328-42846796 | Common:1; Rare:125 | ||||
chr1:42931358-42931532 | Rare:35 | ||||
chr1:42958112-42958408 | Common:6; Rare:108 | ||||
chr1:42958705-42959121 | Common:4; Rare:103; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172557-43172749 | Common:6; Rare:48 | ||||
chr1:43358568-43359010 | Common:7; Rare:140 | ||||
chr1:43367664-43367752 | Common:2; Rare:15 | ||||
chr1:43367920-43368333 | Rare:108 | ||||
chr1:43368365-43368474 | Common:1; Rare:27 | ||||
chr1:43368485-43368761 | Common:1; Rare:34 | ||||
chr1:43389690-43389987 | Common:4; Rare:125; Clinvar:1 | ||||
chr1:43453900-43454108 | Common:2; Rare:52 | ||||
chr1:43454450-43454826 | Rare:85 |