Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15757613-15757974 | Common:2; Rare:56 | ||||
chr1:15758723-15758843 | Common:1; Rare:24 | ||||
chr1:15947090-15947357 | Rare:44 | ||||
chr1:16133238-16133559 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):7 | ||||
chr1:16155995-16156176 | Rare:42; Clinvar:2 | ||||
chr1:16206483-16206719 | Common:6; Rare:48 | ||||
chr1:16352416-16352615 | Common:3; Rare:104 | ||||
chr1:16440653-16440832 | Common:1; Rare:80 | ||||
chr1:16980586-16980782 | Common:4; Rare:70 | ||||
chr1:17439669-17439926 | Rare:86 | ||||
chr1:19210237-19210562 | Common:1; Rare:101 | ||||
chr1:19251510-19251862 | Common:6; Rare:116 | ||||
chr1:19312044-19312355 | Common:8; Rare:149 | ||||
chr1:19419424-19419575 | Rare:33 | ||||
chr1:19485437-19485741 | Common:1; Rare:103 |