Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:72073945-72074365 | Common:2; Rare:146 | ||||
chr16:74368134-74368376 | Common:1; Rare:69 | ||||
chr16:82715880-82716159 | Common:4; Rare:91 | ||||
chr16:84730560-84730787 | Common:3; Rare:57 | ||||
chr17:4999630-4999758 | Common:1; Rare:38 | ||||
chr17:5020538-5020837 | Common:4; Rare:90; Clinvar (benign):5 | ||||
chr17:7310885-7311113 | Rare:51 | ||||
chr17:7834106-7834251 | Rare:50 | ||||
chr17:15786815-15787028 | Common:7; Rare:59 | ||||
chr17:18184862-18185008 | Rare:30 | ||||
chr17:35567990-35568139 | Common:1; Rare:45 | ||||
chr17:38702311-38702479 | Rare:57 | ||||
chr17:39209846-39209900 | Rare:11 | ||||
chr17:41755875-41756197 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):3 | ||||
chr17:43860949-43861136 | Common:1; Rare:35 |