Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:48604764-48605223 | Common:2; Rare:118 | ||||
chr10:49941925-49942281 | Rare:92 | ||||
chr10:50067857-50067999 | Common:2; Rare:68 | ||||
chr10:50623706-50624092 | Common:1; Rare:120 | ||||
chr10:50990622-50990944 | Common:5; Rare:48 | ||||
chr10:51074396-51074612 | Common:1; Rare:52; Clinvar (benign):3 | ||||
chr10:51699486-51699882 | Common:5; Rare:106 | ||||
chr10:52314163-52314333 | Rare:36 | ||||
chr10:52314643-52315074 | Common:3; Rare:105 | ||||
chr10:52315085-52315236 | Common:2; Rare:36 | ||||
chr10:56361195-56361520 | Common:7; Rare:126 | ||||
chr10:58268939-58269278 | Common:6; Rare:108 | ||||
chr10:58385408-58385629 | Common:2; Rare:69 | ||||
chr10:59906132-59906347 | Rare:63 | ||||
chr10:59906407-59906654 | Common:2; Rare:68 |