Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17053957-17054368 | Common:3; Rare:127; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17119445-17119583 | Rare:39 | ||||
chr1:17437601-17438091 | Common:2; Rare:200 | ||||
chr1:17438362-17438654 | Common:5; Rare:110 | ||||
chr1:17439603-17439937 | Rare:110 | ||||
chr1:18901915-18902165 | Common:4; Rare:45 | ||||
chr1:18902446-18903093 | Common:10; Rare:182; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:18956558-18957008 | Common:3; Rare:110 | ||||
chr1:19209661-19209838 | Common:1; Rare:36 | ||||
chr1:19210182-19210668 | Common:1; Rare:145 | ||||
chr1:19251441-19251886 | Common:7; Rare:156 | ||||
chr1:19312018-19312387 | Common:8; Rare:170 | ||||
chr1:19312743-19312914 | Common:3; Rare:36 | ||||
chr1:19485445-19485881 | Rare:158 | ||||
chr1:19485918-19486135 | Common:1; Rare:67 |