Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18039145-18039455 | Common:5; Rare:85; Clinvar (benign):1 | ||||
chr17:18184557-18184667 | Rare:25 | ||||
chr17:18254575-18254824 | Rare:86 | ||||
chr17:18260417-18260668 | Rare:72 | ||||
chr17:18314928-18315317 | Common:1; Rare:110 | ||||
chr17:18781118-18781305 | Common:3; Rare:51 | ||||
chr17:18856195-18856362 | Common:1; Rare:27 | ||||
chr17:19004128-19004322 | Rare:45 | ||||
chr17:19004707-19004878 | Common:1; Rare:54 | ||||
chr17:19362686-19362847 | Rare:65 | ||||
chr17:19377730-19377773 | Common:1; Rare:8 | ||||
chr17:19377898-19378033 | Common:1; Rare:33 | ||||
chr17:19378132-19378545 | Common:2; Rare:99 | ||||
chr17:19648609-19649088 | Common:3; Rare:173; Clinvar (benign):1 | ||||
chr17:21214144-21214355 | Common:2; Rare:95 |