Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:90231111-90231412 | Common:2; Rare:105 | ||||
chr15:96327340-96327499 | Common:3; Rare:20 | ||||
chr16:9068403-9068563 | Common:2; Rare:42 | ||||
chr16:29220202-29220425 | Common:1; Rare:51 | ||||
chr16:30444544-30444614 | Rare:12 | ||||
chr16:30875333-30875441 | Rare:31 | ||||
chr16:56617381-56617668 | Common:4; Rare:58 | ||||
chr17:1712015-1712098 | Rare:21 | ||||
chr17:7478999-7479047 | Rare:7 | ||||
chr17:44351430-44351638 | Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr17:68044010-68044372 | Common:2; Rare:99 | ||||
chr17:76557676-76557848 | Rare:61 | ||||
chr17:82845453-82845604 | Common:9; Rare:30 | ||||
chr18:5238006-5238151 | Common:1; Rare:55 | ||||
chr18:59355352-59355521 | Rare:51; Clinvar (benign):1 |