Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:169765058-169765197 | Rare:63; Clinvar (pathogenic):1 | ||||
chr3:171874260-171874557 | Common:3; Rare:52 | ||||
chr3:183269447-183269560 | Rare:21 | ||||
chr3:184317341-184317729 | Common:2; Rare:109 | ||||
chr3:184322700-184322954 | Rare:64 | ||||
chr3:194134919-194135223 | Rare:103 | ||||
chr3:195657809-195658122 | Common:13; Rare:47 | ||||
chr3:195990216-195990419 | Rare:24 | ||||
chr3:197627841-197628009 | Common:6; Rare:60 | ||||
chr4:38055971-38056099 | Common:1; Rare:23 | ||||
chr4:38056106-38056243 | Rare:20 | ||||
chr4:55947894-55948176 | Common:2; Rare:46 | ||||
chr4:76306558-76306696 | Rare:39 | ||||
chr4:77011174-77011280 | Rare:21 | ||||
chr4:84870488-84870618 | Rare:24 |