Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:72664968-72665158 | Rare:62 | ||||
chr16:74368127-74368342 | Common:1; Rare:63 | ||||
chr16:75631169-75631502 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):3 | ||||
chr17:870262-870461 | Common:3; Rare:46 | ||||
chr17:2848812-2848988 | Common:2; Rare:43 | ||||
chr17:17836255-17836429 | Common:2; Rare:43 | ||||
chr17:48646714-48646793 | Rare:24 | ||||
chr17:48646811-48646901 | Common:3; Rare:24 | ||||
chr17:64145760-64145975 | Common:2; Rare:56 | ||||
chr17:64975564-64975712 | Common:1; Rare:50 | ||||
chr17:76557637-76557832 | Common:1; Rare:69 | ||||
chr18:3593953-3594127 | Common:3; Rare:29 | ||||
chr18:3603493-3603744 | Common:1; Rare:40 | ||||
chr18:5238038-5238125 | Common:1; Rare:36 | ||||
chr18:28115174-28115449 | Rare:49 |