Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244863715-244863911 | Rare:63; Clinvar:2; Clinvar (benign):3 | ||||
chr10:661474-661552 | Common:1; Rare:20 | ||||
chr10:5023248-5023597 | Common:2; Rare:67 | ||||
chr10:5099169-5099462 | Common:4; Rare:104 | ||||
chr10:5766055-5766217 | Common:1; Rare:38 | ||||
chr10:5915966-5916336 | Common:2; Rare:73 | ||||
chr10:6163635-6163887 | Common:6; Rare:89 | ||||
chr10:6404762-6404949 | Common:4; Rare:34 | ||||
chr10:10798363-10798650 | Common:4; Rare:63 | ||||
chr10:12172802-12172998 | Rare:60 | ||||
chr10:17011987-17012020 | Rare:7 | ||||
chr10:18520851-18521100 | Rare:55 | ||||
chr10:18533901-18534209 | Common:1; Rare:88; Clinvar:10; Clinvar (benign):1 | ||||
chr10:19817683-19817979 | Common:2; Rare:64 | ||||
chr10:20072039-20072424 | Common:6; Rare:79 |