Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8816744-8816873 | Rare:23 | ||||
chr1:8870435-8870536 | Common:1; Rare:25 | ||||
chr1:8870635-8870779 | Common:1; Rare:39 | ||||
chr1:9166266-9166586 | Common:3; Rare:60 | ||||
chr1:9182104-9182222 | Rare:30 | ||||
chr1:9191611-9191811 | Common:1; Rare:45 | ||||
chr1:9198698-9198969 | Common:2; Rare:72 | ||||
chr1:9428929-9429133 | Common:2; Rare:61 | ||||
chr1:10130571-10130816 | Common:2; Rare:55 | ||||
chr1:10431871-10432070 | Common:3; Rare:40 | ||||
chr1:11938504-11938584 | Common:1; Rare:16 | ||||
chr1:11947689-11948065 | Rare:91; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:12619099-12619253 | Rare:39 | ||||
chr1:15060067-15060194 | Common:2; Rare:34 | ||||
chr1:15065277-15065576 | Rare:47 |