Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19210238-19210538 | Common:1; Rare:96 | ||||
chr1:19251494-19251856 | Common:6; Rare:122 | ||||
chr1:19288710-19288837 | Common:5; Rare:50 | ||||
chr1:19312046-19312350 | Common:8; Rare:148 | ||||
chr1:19485437-19485775 | Common:1; Rare:126 | ||||
chr1:19596657-19597096 | Common:4; Rare:147 | ||||
chr1:20486186-20486363 | Rare:39 | ||||
chr1:20661340-20661682 | Common:3; Rare:123; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786564-20786839 | Rare:100 | ||||
chr1:20787196-20787437 | Rare:113 | ||||
chr1:21176836-21177053 | Rare:62 | ||||
chr1:21290447-21290770 | Common:2; Rare:80 | ||||
chr1:21345467-21345704 | Common:3; Rare:88 | ||||
chr1:21551042-21551384 | Common:1; Rare:67 | ||||
chr1:21783086-21783289 | Common:2; Rare:73 |