Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29996064-29996302 | Common:2; Rare:85 | ||||
chr16:30064340-30064480 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr16:30065566-30065921 | Rare:122 | ||||
chr16:30069659-30069984 | Common:1; Rare:114; Clinvar:3; Clinvar (benign):6 | ||||
chr16:30075894-30076055 | Rare:55 | ||||
chr16:30123043-30123371 | Common:6; Rare:94 | ||||
chr16:30355210-30355488 | Common:2; Rare:91 | ||||
chr16:30445871-30446055 | Common:1; Rare:45 | ||||
chr16:30526772-30526936 | Common:4; Rare:49 | ||||
chr16:30534535-30534616 | Common:1; Rare:32 | ||||
chr16:30534799-30535089 | Common:3; Rare:92 | ||||
chr16:30572143-30572247 | Rare:29 | ||||
chr16:30650542-30650826 | Rare:58 | ||||
chr16:30697934-30698235 | Common:1; Rare:133 | ||||
chr16:30698452-30698598 | Common:1; Rare:62 |