Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151346852-151346955 | Rare:27 | ||||
chr1:151347239-151347476 | Rare:54 | ||||
chr1:151716642-151717130 | Common:1; Rare:127 | ||||
chr1:151763451-151763555 | Common:1; Rare:37 | ||||
chr1:151790436-151790709 | Common:1; Rare:69 | ||||
chr1:153670916-153671247 | Rare:112 | ||||
chr1:153727746-153728092 | Common:1; Rare:103 | ||||
chr1:153958584-153958877 | Common:1; Rare:88 | ||||
chr1:153963476-153963719 | Common:2; Rare:65 | ||||
chr1:153967619-153967908 | Common:1; Rare:52 | ||||
chr1:153986226-153986403 | Rare:42 | ||||
chr1:153990605-153990826 | Common:2; Rare:94 | ||||
chr1:154182986-154183286 | Rare:96 | ||||
chr1:154220545-154221001 | Common:1; Rare:152 | ||||
chr1:154272421-154272672 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):2 |