Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:96770337-96770545 | Common:1; Rare:38 | ||||
chr5:98774441-98774636 | Rare:58 | ||||
chr5:128083040-128083179 | Common:8; Rare:45 | ||||
chr5:134436521-134436717 | Rare:29 | ||||
chr5:137316015-137316230 | Rare:39 | ||||
chr5:137870225-137870725 | Common:3; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
chr5:139394740-139394924 | Rare:58 | ||||
chr5:141618084-141618407 | Common:2; Rare:77 | ||||
chr5:143057192-143057495 | Common:1; Rare:54 | ||||
chr5:143135896-143136135 | Common:1; Rare:46 | ||||
chr5:148826431-148826632 | Common:2; Rare:56 | ||||
chr5:149180554-149180598 | Rare:6 | ||||
chr5:150778638-150778864 | Common:1; Rare:88 | ||||
chr5:150779962-150780146 | Rare:33 | ||||
chr5:150946524-150946840 | Common:1; Rare:69 |