Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:47228875-47229240 | Rare:122 | ||||
chr1:47229218-47230120 | Common:8; Rare:531 | ||||
chr1:47230691-47231188 | Common:9; Rare:253 | ||||
chr1:47231103-47232068 | Common:20; Rare:600 | ||||
chr1:47232086-47232570 | Rare:561 | ||||
chr1:47313400-47313800 | Common:3; Rare:107 | ||||
chr1:47313936-47314765 | Common:29; Rare:798; Clinvar:16; Clinvar (benign):3 | ||||
chr1:47333045-47333445 | Common:2; Rare:67 | ||||
chr1:47333613-47334024 | Common:20; Rare:759 | ||||
chr1:47334031-47334431 | Common:9; Rare:331 | ||||
chr1:48472129-48472529 | Common:16; Rare:339 | ||||
chr1:50958856-50959550 | Common:14; Rare:238 | ||||
chr1:50959788-50960040 | Common:7; Rare:203 | ||||
chr1:50960022-50960736 | Common:3; Rare:791 | ||||
chr1:50967860-50968390 | Common:4; Rare:234 |