Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4942403-4942664 | Common:1; Rare:92 | ||||
chr17:4946632-4946991 | Common:1; Rare:89 | ||||
chr17:4948932-4949181 | Common:2; Rare:85 | ||||
chr17:4950486-4950596 | Rare:28 | ||||
chr17:4950826-4951141 | Common:1; Rare:69; Clinvar (benign):1 | ||||
chr17:4967725-4967909 | Rare:80 | ||||
chr17:4987625-4987814 | Common:2; Rare:65 | ||||
chr17:4997933-4998154 | Common:2; Rare:88; Clinvar (benign):1 | ||||
chr17:5191838-5192047 | Rare:69 | ||||
chr17:5234788-5234983 | Rare:45 | ||||
chr17:5419358-5419368 | Rare:4 | ||||
chr17:5419608-5420225 | Common:6; Rare:202 | ||||
chr17:5433079-5433390 | Common:1; Rare:103; Clinvar (pathogenic):2 | ||||
chr17:5486144-5486602 | Common:5; Rare:159 | ||||
chr17:5486810-5486920 | Common:3; Rare:34 |