Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20469170-20469471 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
chr14:20684418-20684756 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
chr14:20802795-20802970 | Common:1; Rare:23 | ||||
chr14:20955434-20955474 | Common:1; Rare:6 | ||||
chr14:21024965-21025190 | Rare:84 | ||||
chr14:21025697-21025809 | Rare:22 | ||||
chr14:21070847-21071015 | Rare:34 | ||||
chr14:21100985-21101172 | Rare:23 | ||||
chr14:21104708-21104727 | Rare:3 | ||||
chr14:21383931-21384286 | Common:8; Rare:118 | ||||
chr14:21437221-21437396 | Common:3; Rare:75 | ||||
chr14:21456040-21456134 | Common:2; Rare:23 | ||||
chr14:21476587-21476784 | Rare:86 | ||||
chr14:21476826-21477271 | Common:2; Rare:145 | ||||
chr14:21511237-21511513 | Rare:85 |