Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:14598391-14598691 | Common:1; Rare:90 | ||||
chr1:15526553-15526885 | Common:2; Rare:102 | ||||
chr1:16352418-16352525 | Rare:56 | ||||
chr1:16440601-16440753 | Rare:44 | ||||
chr1:16613508-16613660 | |||||
chr1:17054009-17054320 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
chr1:19210238-19210417 | Rare:68 | ||||
chr1:19251505-19251892 | Common:8; Rare:135 | ||||
chr1:19312053-19312321 | Common:8; Rare:134 | ||||
chr1:19485449-19485762 | Rare:116 | ||||
chr1:19596815-19597068 | Common:3; Rare:105 | ||||
chr1:20486191-20486338 | Rare:33 | ||||
chr1:20508117-20508205 | Rare:23 | ||||
chr1:20661331-20661692 | Common:3; Rare:131; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21345463-21345678 | Common:2; Rare:82 |