Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153783751-153783855 | Common:3; Rare:35 | ||||
chr1:154869488-154869647 | Rare:43 | ||||
chr1:155194704-155194807 | Common:1; Rare:33 | ||||
chr1:155343654-155343904 | Common:1; Rare:61 | ||||
chr1:156130320-156130771 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156456530-156456774 | Rare:55 | ||||
chr1:160212933-160213182 | Rare:44 | ||||
chr1:161390013-161390309 | Common:8; Rare:62 | ||||
chr1:161530882-161531129 | Common:5; Rare:106 | ||||
chr1:165682201-165682321 | Common:1; Rare:27 | ||||
chr1:167221964-167222081 | Rare:44 | ||||
chr1:167454955-167455105 | Rare:28 | ||||
chr1:168056424-168056614 | Common:1; Rare:35 | ||||
chr1:172144597-172144939 | Rare:60 | ||||
chr1:173865528-173865769 | Common:1; Rare:81 |