Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:211382654-211382865 | Common:2; Rare:86 | ||||
chr1:211538480-211538563 | Rare:12 | ||||
chr1:211829440-211829480 | Common:1; Rare:12 | ||||
chr1:212306040-212306058 | Rare:5 | ||||
chr1:213399746-213399982 | Common:1; Rare:48 | ||||
chr1:218345216-218345646 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
chr1:218345654-218345695 | Common:1; Rare:8; Clinvar (benign):1 | ||||
chr1:218348010-218348305 | Common:4; Rare:68 | ||||
chr1:218699966-218700223 | Common:1; Rare:50 | ||||
chr1:220253958-220254032 | Rare:19 | ||||
chr1:221511150-221511438 | Common:1; Rare:41 | ||||
chr1:222814971-222815157 | Common:2; Rare:68 | ||||
chr1:223027875-223027937 | Common:2; Rare:17 | ||||
chr1:223992559-223993001 | Common:5; Rare:127 | ||||
chr1:228369206-228369452 | Common:1; Rare:42 |