Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34874172-34874232 | Common:1; Rare:19 | ||||
chr14:35402110-35402671 | Common:4; Rare:160; Clinvar:3; Clinvar (benign):2 | ||||
chr14:39589152-39589249 | Rare:28 | ||||
chr14:49633870-49634043 | Common:1; Rare:69; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:49789563-49789625 | Rare:16 | ||||
chr14:49803843-49803974 | Rare:23 | ||||
chr14:49814019-49814323 | Common:2; Rare:76 | ||||
chr14:49862645-49863039 | Common:1; Rare:182 | ||||
chr14:50414129-50414382 | Common:3; Rare:95 | ||||
chr14:50761808-50762183 | Common:3; Rare:87 | ||||
chr14:51641932-51642178 | Common:2; Rare:37 | ||||
chr14:58266574-58266852 | Common:2; Rare:48 | ||||
chr14:58267122-58267507 | Common:2; Rare:90 | ||||
chr14:59277929-59278155 | Rare:44 | ||||
chr14:64126388-64126754 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):4 |