Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7561803-7562011 | Common:2; Rare:56 | ||||
chr17:7579459-7579722 | Common:1; Rare:83 | ||||
chr17:7583510-7583868 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7614860-7615152 | Rare:85 | ||||
chr17:7843663-7843733 | Rare:25 | ||||
chr17:7843950-7844303 | Common:5; Rare:90 | ||||
chr17:7857096-7857392 | Common:2; Rare:144 | ||||
chr17:7857449-7858074 | Common:4; Rare:202 | ||||
chr17:7885187-7885343 | Rare:43 | ||||
chr17:7931906-7932235 | Common:5; Rare:90 | ||||
chr17:8147555-8148022 | Common:1; Rare:164 | ||||
chr17:8151174-8151491 | Common:3; Rare:80 | ||||
chr17:8152348-8152726 | Common:4; Rare:89 | ||||
chr17:8162911-8163079 | Rare:52 | ||||
chr17:8248042-8248181 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 |