Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15835794-15836134 | Common:6; Rare:164 | ||||
chr1:16155014-16155235 | Rare:46 | ||||
chr1:16499246-16499428 | Common:1; Rare:86 | ||||
chr1:16644637-16644790 | Common:1; Rare:2 | ||||
chr1:16765256-16765443 | Rare:8 | ||||
chr1:16889642-16889687 | Common:1; Rare:13 | ||||
chr1:16895690-16895980 | Common:4; Rare:56 | ||||
chr1:16913863-16914121 | Common:8; Rare:54 | ||||
chr1:19201704-19201734 | Rare:5 | ||||
chr1:19238101-19238261 | Common:1; Rare:39 | ||||
chr1:21261851-21262088 | Common:2; Rare:52 | ||||
chr1:21831462-21831757 | Common:2; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
chr1:21857014-21857325 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):2 | ||||
chr1:21884826-21885046 | Rare:59; Clinvar:1 | ||||
chr1:22025188-22025558 | Common:8; Rare:97 |