Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:89534115-89534372 | Rare:32 | ||||
chr10:91807531-91807691 | Rare:27 | ||||
chr10:95389743-95389890 | Rare:31 | ||||
chr10:96090198-96090291 | Common:1; Rare:39 | ||||
chr10:97788997-97789346 | Rare:73 | ||||
chr10:101694426-101694665 | Common:3; Rare:80; Clinvar:3; Clinvar (benign):4 | ||||
chr10:103659863-103660154 | Common:1; Rare:63 | ||||
chr10:110870998-110871235 | Common:1; Rare:40 | ||||
chr10:116542097-116542414 | Common:1; Rare:47 | ||||
chr10:116546752-116547000 | Common:1; Rare:39 | ||||
chr10:116553610-116553891 | Common:1; Rare:91; Clinvar:1 | ||||
chr10:116554442-116554516 | Rare:14 | ||||
chr10:116554784-116555004 | Rare:43 | ||||
chr10:116555169-116555507 | Common:1; Rare:98; Clinvar (pathogenic):1 | ||||
chr10:116593377-116593619 | Rare:36 |