Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:31318429-31318760 | Rare:110; Clinvar (benign):1 | ||||
chr17:31487760-31488148 | Rare:124 | ||||
chr17:31488473-31488482 | Rare:1 | ||||
chr17:31859215-31859469 | Common:2; Rare:70 | ||||
chr17:31901594-31901992 | Common:3; Rare:118 | ||||
chr17:31936706-31937092 | Common:1; Rare:112 | ||||
chr17:32007260-32007476 | Rare:63 | ||||
chr17:32142037-32142148 | Common:1; Rare:27 | ||||
chr17:32142157-32142732 | Common:8; Rare:189 | ||||
chr17:32341802-32342312 | Common:2; Rare:132 | ||||
chr17:32349954-32350212 | Rare:120 | ||||
chr17:32350497-32350934 | Rare:109 | ||||
chr17:32444238-32444580 | Common:1; Rare:120 | ||||
chr17:32445264-32445328 | Common:1; Rare:3 | ||||
chr17:32486443-32486739 | Common:1; Rare:110 |