Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16613189-16613400 | Common:2; Rare:2 | ||||
chr1:16613508-16613680 | Common:1; Rare:1 | ||||
chr1:17011865-17012100 | Common:1; Rare:67; Clinvar:2 | ||||
chr1:17053933-17054325 | Common:3; Rare:124; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr1:17119448-17119653 | Rare:53 | ||||
chr1:17437604-17438094 | Common:2; Rare:201 | ||||
chr1:17438493-17438828 | Common:2; Rare:116 | ||||
chr1:17439643-17439918 | Rare:94 | ||||
chr1:18902088-18902143 | Rare:10 | ||||
chr1:18902503-18903087 | Common:9; Rare:164; Clinvar:9 | ||||
chr1:18956575-18956972 | Common:3; Rare:103 | ||||
chr1:19209707-19209925 | Common:1; Rare:49 | ||||
chr1:19210222-19210638 | Common:1; Rare:128 | ||||
chr1:19251457-19251879 | Common:6; Rare:147 | ||||
chr1:19312017-19312391 | Common:9; Rare:171 |