Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101710124-101710147 | Rare:5 | ||||
chr10:101779234-101779268 | Rare:5 | ||||
chr10:101814857-101815019 | Rare:33 | ||||
chr10:101831027-101831132 | Rare:28 | ||||
chr10:101840798-101840925 | Rare:22 | ||||
chr10:101858781-101859036 | Rare:38 | ||||
chr10:101901527-101901629 | Common:1; Rare:17 | ||||
chr10:101903881-101904221 | Rare:49 | ||||
chr10:101968439-101968521 | Common:1; Rare:8 | ||||
chr10:102117888-102118037 | Common:1; Rare:31 | ||||
chr10:102133714-102133811 | Rare:21 | ||||
chr10:102189542-102189682 | Rare:19 | ||||
chr10:102399534-102399660 | Rare:47; Clinvar (benign):1 | ||||
chr10:102435529-102435974 | Rare:62 | ||||
chr10:102449710-102450130 | Common:1; Rare:88 |