Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:40954367-40954743 | Common:4; Rare:136 | ||||
chr14:47541779-47542025 | Common:1; Rare:57 | ||||
chr14:47675606-47675714 | Common:1; Rare:25 | ||||
chr14:49633531-49633737 | Common:1; Rare:84; Clinvar:8; Clinvar (benign):5 | ||||
chr14:49633917-49634053 | Common:1; Rare:59; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49862303-49862559 | Common:1; Rare:57 | ||||
chr14:49862642-49863014 | Common:1; Rare:172 | ||||
chr14:52553948-52554071 | Common:1; Rare:24 | ||||
chr14:58511960-58512241 | Common:1; Rare:43 | ||||
chr14:59189969-59189993 | Rare:4 | ||||
chr14:59463911-59464051 | Rare:63 | ||||
chr14:62117161-62117519 | Common:2; Rare:69 | ||||
chr14:69091608-69091762 | Rare:29 | ||||
chr14:69237151-69237395 | Common:2; Rare:48 | ||||
chr14:69547949-69548169 | Common:4; Rare:45 |