Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113351538-113351746 | Common:1; Rare:41 | ||||
chr14:20971722-20971975 | Common:3; Rare:38 | ||||
chr14:24181734-24182024 | Rare:93 | ||||
chr14:32152207-32152521 | Common:2; Rare:69 | ||||
chr14:32203245-32203664 | Common:13; Rare:186 | ||||
chr14:34874137-34874206 | Common:1; Rare:18 | ||||
chr14:35402003-35402102 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
chr14:41604777-41605016 | Common:4; Rare:47 | ||||
chr14:41605314-41605376 | Common:2; Rare:12 | ||||
chr14:48998305-48998463 | Rare:26 | ||||
chr14:49633848-49634080 | Common:1; Rare:85; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr14:49862639-49863039 | Common:1; Rare:182 | ||||
chr14:49868119-49868367 | Common:1; Rare:52 | ||||
chr14:50003406-50003540 | Rare:37 | ||||
chr14:52001720-52001864 | Rare:37 |