Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:45135706-45136037 | Common:1; Rare:80 | ||||
chr14:45136154-45136241 | Rare:27; Clinvar:2 | ||||
chr14:45253010-45253433 | Common:1; Rare:122 | ||||
chr14:45253512-45253644 | Common:1; Rare:51 | ||||
chr14:49586289-49586605 | Common:1; Rare:130; Clinvar (benign):1 | ||||
chr14:49598500-49598789 | Common:3; Rare:118 | ||||
chr14:49598800-49599078 | Common:1; Rare:96 | ||||
chr14:49599091-49599390 | Rare:85 | ||||
chr14:49600201-49600232 | Rare:8 | ||||
chr14:49620216-49620406 | Rare:53 | ||||
chr14:49620537-49621033 | Common:3; Rare:178; Clinvar:7; Clinvar (benign):1 | ||||
chr14:49621116-49621329 | Rare:69; Clinvar:2 | ||||
chr14:49634201-49634761 | Common:2; Rare:251; Clinvar:19; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:49688097-49688389 | Common:2; Rare:107 | ||||
chr14:49692979-49693066 | Rare:26 |