Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81220834-81221046 | Common:1; Rare:102 | ||||
chr14:90396870-90396978 | Rare:51 | ||||
chr14:90396991-90397232 | Common:5; Rare:119; Clinvar (benign):2 | ||||
chr14:90404475-90404694 | Rare:54; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:91947657-91947806 | Common:1; Rare:46; Clinvar (benign):2 | ||||
chr14:92040019-92040187 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr14:92121649-92122014 | Common:5; Rare:126 | ||||
chr14:92793953-92794253 | Rare:88 | ||||
chr14:93115240-93115451 | Common:1; Rare:79 | ||||
chr14:93184834-93185019 | Rare:65 | ||||
chr14:93206983-93207294 | Common:2; Rare:152 | ||||
chr14:93976442-93976674 | Rare:49 | ||||
chr14:93976701-93976770 | Rare:13 | ||||
chr14:94081123-94081333 | Common:5; Rare:69 | ||||
chr14:95157424-95157711 | Common:4; Rare:102 |