Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:6634062-6634164 | Rare:22 | ||||
chr10:7806843-7807159 | Common:1; Rare:55 | ||||
chr10:8018985-8018994 | Rare:3 | ||||
chr10:13349987-13350206 | Common:2; Rare:53 | ||||
chr10:13700896-13700953 | Rare:11 | ||||
chr10:13838136-13838244 | Common:1; Rare:16 | ||||
chr10:13891718-13892029 | Common:3; Rare:98 | ||||
chr10:14185408-14185466 | Common:5; Rare:35 | ||||
chr10:14909162-14909450 | Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
chr10:19817673-19817847 | Common:1; Rare:38 | ||||
chr10:20120145-20120187 | Rare:11 | ||||
chr10:20370312-20370609 | Common:4; Rare:69 | ||||
chr10:20953121-20953340 | Common:1; Rare:30 | ||||
chr10:21030293-21030477 | Common:1; Rare:29 | ||||
chr10:21282048-21282442 | Common:2; Rare:67 |