Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7583749-7583858 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
chr17:7857198-7857495 | Common:2; Rare:138 | ||||
chr17:7857508-7857625 | Common:1; Rare:35 | ||||
chr17:7931914-7932235 | Common:5; Rare:87 | ||||
chr17:8162937-8163081 | Rare:41 | ||||
chr17:8176342-8176492 | Rare:46 | ||||
chr17:9900990-9901224 | Common:3; Rare:74 | ||||
chr17:10697505-10697648 | Common:3; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069440-14069549 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15999611-15999824 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):4 | ||||
chr17:16040440-16040582 | Rare:25 | ||||
chr17:18183693-18183925 | Rare:105 | ||||
chr17:18314953-18315305 | Rare:100 | ||||
chr17:18781103-18781301 | Common:4; Rare:54 | ||||
chr17:19648611-19648771 | Common:2; Rare:51 |