Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6651553-6651720 | Common:1; Rare:63 | ||||
chr17:7012314-7012705 | Rare:131 | ||||
chr17:7251963-7252219 | Rare:100 | ||||
chr17:7315112-7315429 | Common:4; Rare:113 | ||||
chr17:7404770-7404926 | Common:3; Rare:38 | ||||
chr17:7479557-7479709 | Rare:23 | ||||
chr17:7484244-7484387 | Common:1; Rare:63 | ||||
chr17:7484690-7484813 | Rare:55 | ||||
chr17:7583530-7583858 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7584070-7584126 | Rare:11 | ||||
chr17:7686424-7686677 | Rare:62 | ||||
chr17:7857383-7857662 | Common:2; Rare:95 | ||||
chr17:7857900-7858087 | Rare:66 | ||||
chr17:7885179-7885346 | Rare:49 | ||||
chr17:7885473-7885656 | Rare:36 |