Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:99645335-99645535 | Common:1; Rare:39 | ||||
chr1:99645565-99645867 | Rare:39 | ||||
chr1:99645871-99645938 | Rare:14 | ||||
chr1:99645986-99646431 | Common:1; Rare:91 | ||||
chr1:99850005-99850455 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):2 | ||||
chr1:99969922-99970098 | Rare:47 | ||||
chr1:100037967-100038193 | Common:1; Rare:90 | ||||
chr1:100132908-100133216 | Common:2; Rare:112 | ||||
chr1:100249805-100250017 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266107-100266357 | Common:3; Rare:87 | ||||
chr1:100352175-100352516 | Common:1; Rare:80 | ||||
chr1:100894778-100894914 | Common:1; Rare:29 | ||||
chr1:100895958-100896197 | Rare:60 | ||||
chr1:101025763-101025931 | Common:1; Rare:50 | ||||
chr1:101236611-101237072 | Common:5; Rare:95 |