Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48048619-48048864 | Common:3; Rare:39 | ||||
chr17:48101141-48101243 | Rare:27 | ||||
chr17:48107427-48107595 | Common:3; Rare:40 | ||||
chr17:48544588-48544696 | Rare:60 | ||||
chr17:48944773-48944901 | Common:1; Rare:42 | ||||
chr17:49210228-49210436 | Common:2; Rare:30 | ||||
chr17:49210591-49210712 | Rare:19 | ||||
chr17:49230768-49230881 | Common:2; Rare:27 | ||||
chr17:49707877-49708240 | Rare:156 | ||||
chr17:49788576-49788724 | Common:1; Rare:45 | ||||
chr17:50165697-50166052 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
chr17:50188742-50189011 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr17:50719452-50719654 | Rare:79 | ||||
chr17:50866351-50866560 | Common:2; Rare:65 | ||||
chr17:51120734-51121043 | Rare:124 |