Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19210244-19210552 | Common:1; Rare:98 | ||||
chr1:19251498-19251874 | Common:6; Rare:126 | ||||
chr1:19311970-19312358 | Common:8; Rare:174 | ||||
chr1:19485435-19485762 | Common:1; Rare:122 | ||||
chr1:19596869-19597123 | Common:2; Rare:115 | ||||
chr1:19799670-19799987 | Common:5; Rare:98 | ||||
chr1:20070023-20070350 | Common:3; Rare:65 | ||||
chr1:20186008-20186141 | Rare:43 | ||||
chr1:20508020-20508194 | Common:2; Rare:60 | ||||
chr1:20661206-20661245 | Rare:13 | ||||
chr1:20661346-20661705 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786573-20786832 | Rare:95 | ||||
chr1:20787196-20787447 | Rare:117 | ||||
chr1:21176848-21177039 | Rare:53 | ||||
chr1:21290203-21290505 | Common:1; Rare:66 |