Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15976072-15976185 | Common:2; Rare:23 | ||||
chr1:16352413-16352548 | Common:1; Rare:69 | ||||
chr1:16440492-16440759 | Common:2; Rare:71 | ||||
chr1:17053983-17054317 | Common:3; Rare:104; Clinvar:10; Clinvar (benign):9 | ||||
chr1:17119448-17119569 | Rare:32 | ||||
chr1:19210076-19210505 | Rare:146 | ||||
chr1:19251494-19251842 | Common:6; Rare:117 | ||||
chr1:19312013-19312333 | Common:8; Rare:153 | ||||
chr1:19596856-19597064 | Common:2; Rare:93 | ||||
chr1:20486179-20486363 | Rare:41 | ||||
chr1:20508079-20508187 | Common:2; Rare:42 | ||||
chr1:20661340-20661687 | Common:3; Rare:125; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787196-20787437 | Rare:113 | ||||
chr1:21176848-21177074 | Rare:63 | ||||
chr1:21345476-21345663 | Common:1; Rare:73 |