Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:92121655-92121990 | Common:5; Rare:110 | ||||
chr14:93184856-93185001 | Rare:45 | ||||
chr14:93207006-93207284 | Common:2; Rare:136 | ||||
chr14:94081141-94081341 | Common:4; Rare:67 | ||||
chr14:96363333-96363552 | Common:1; Rare:71 | ||||
chr14:96502286-96502442 | Rare:60 | ||||
chr14:99480786-99480995 | Common:2; Rare:82 | ||||
chr14:100375331-100375755 | Common:4; Rare:71 | ||||
chr14:100376264-100376535 | Common:3; Rare:87 | ||||
chr14:101809736-101809880 | Rare:26 | ||||
chr14:102139678-102139920 | Rare:83 | ||||
chr14:102362858-102363092 | Rare:105 | ||||
chr14:103333909-103334252 | Common:3; Rare:142 | ||||
chr14:103528981-103529205 | Common:1; Rare:56 | ||||
chr14:103562624-103563013 | Common:6; Rare:139; Clinvar (benign):2 |