Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94409344-94409605 | Rare:75; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr7:94410238-94410527 | Rare:62; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr7:94421505-94421745 | Rare:40 | ||||
chr7:99141867-99142019 | Rare:33 | ||||
chr7:100335876-100336149 | Common:1; Rare:89 | ||||
chr7:100607636-100608057 | Common:2; Rare:126 | ||||
chr7:100681897-100682154 | Rare:93 | ||||
chr7:103311878-103312080 | Rare:57 | ||||
chr7:103322019-103322235 | Common:1; Rare:58 | ||||
chr7:103326635-103326951 | Rare:59 | ||||
chr7:105013039-105013223 | Common:1; Rare:67 | ||||
chr7:105013592-105013670 | Rare:32 | ||||
chr7:106659017-106659103 | Rare:16 | ||||
chr7:107924011-107924297 | Common:3; Rare:93; Clinvar:1; Clinvar (benign):5 | ||||
chr7:116327885-116328047 | Common:1; Rare:29 |