Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30657832-30658504 | Common:2; Rare:165 | ||||
chr16:30658538-30659430 | Common:1; Rare:297 | ||||
chr16:30659802-30660374 | Common:4; Rare:180 | ||||
chr16:30660788-30660974 | Rare:40 | ||||
chr16:30697966-30698307 | Common:1; Rare:147 | ||||
chr16:30698322-30698735 | Common:1; Rare:153 | ||||
chr16:30698880-30699409 | Common:1; Rare:155; Clinvar (benign):1 | ||||
chr16:30748062-30748523 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):3 | ||||
chr16:30748748-30748823 | Rare:25 | ||||
chr16:30761409-30761636 | Rare:86 | ||||
chr16:30762035-30762382 | Common:3; Rare:113 | ||||
chr16:30787124-30787256 | Rare:20 | ||||
chr16:30893937-30894417 | Common:5; Rare:128 | ||||
chr16:30897011-30897384 | Common:1; Rare:61 | ||||
chr16:30922551-30922877 | Common:1; Rare:91 |