Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23559335-23559661 | Common:2; Rare:140 | ||||
chr1:23691613-23691836 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr1:23743302-23743505 | Rare:79 | ||||
chr1:23778288-23778517 | Common:9; Rare:119 | ||||
chr1:23791047-23791225 | Rare:55 | ||||
chr1:23800732-23800984 | Common:1; Rare:92 | ||||
chr1:23959641-23959908 | Common:2; Rare:72 | ||||
chr1:24642971-24643335 | Common:2; Rare:113 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247441-25247621 | Common:2; Rare:59 | ||||
chr1:25338206-25338447 | Common:1; Rare:84 | ||||
chr1:25819858-25820015 | Common:2; Rare:49 | ||||
chr1:25859370-25859580 | Common:2; Rare:85 | ||||
chr1:25906397-25906573 | Rare:71 | ||||
chr1:26234005-26234226 | Common:1; Rare:74 |