Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19308549-19308773 | Common:2; Rare:58 | ||||
chr1:19311958-19312350 | Common:8; Rare:174 | ||||
chr1:19484117-19484237 | Common:1; Rare:40 | ||||
chr1:19485446-19485749 | Rare:107 | ||||
chr1:19596767-19597102 | Common:3; Rare:127 | ||||
chr1:19643622-19643763 | Common:1; Rare:21 | ||||
chr1:19799853-19800215 | Common:5; Rare:97 | ||||
chr1:19882393-19882428 | Rare:16 | ||||
chr1:20186083-20186138 | Rare:18 | ||||
chr1:20486179-20486384 | Rare:50 | ||||
chr1:20508031-20508216 | Common:2; Rare:64 | ||||
chr1:20661346-20661682 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786564-20786837 | Rare:99 | ||||
chr1:20787196-20787417 | Rare:107 | ||||
chr1:21176848-21177153 | Common:1; Rare:91 |