Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:47232153-47232485 | Rare:83 | ||||
chr1:47312883-47313021 | Rare:20 | ||||
chr1:47313948-47314443 | Common:5; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
chr1:47333624-47333726 | Rare:24 | ||||
chr1:47333732-47334111 | Common:3; Rare:118 | ||||
chr1:47334198-47334305 | Rare:34 | ||||
chr1:48472141-48472440 | Common:4; Rare:90 | ||||
chr1:50959762-50959959 | Common:2; Rare:65 | ||||
chr1:50960059-50960354 | Rare:87 | ||||
chr1:50969992-50970423 | Common:1; Rare:92 | ||||
chr1:51236193-51236570 | Common:4; Rare:119 | ||||
chr1:51519217-51519381 | Common:6; Rare:56 | ||||
chr1:51729666-51730092 | Common:2; Rare:123 | ||||
chr1:51750164-51750410 | Rare:48 | ||||
chr1:51789686-51789905 | Common:1; Rare:43 |