Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:45149258-45149451 | Rare:68 | ||||
chr17:45150224-45150313 | Rare:39 | ||||
chr17:45247654-45247970 | Common:1; Rare:62 | ||||
chr17:47678041-47678410 | Common:1; Rare:50 | ||||
chr17:48546400-48546700 | Rare:56 | ||||
chr17:48552830-48553023 | Rare:46 | ||||
chr17:48936194-48936512 | Common:1; Rare:50 | ||||
chr17:50189375-50190111 | Common:4; Rare:180; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
chr17:50197730-50198004 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):6 | ||||
chr17:58324408-58324482 | Rare:20 | ||||
chr17:59910383-59910598 | Rare:36 | ||||
chr17:60087152-60087164 | Rare:3 | ||||
chr17:60134868-60135039 | Rare:27 | ||||
chr17:64722815-64722937 | Common:1; Rare:21 | ||||
chr17:68044066-68044356 | Common:1; Rare:75 |