Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73785936-73786033 | Rare:19 | ||||
chr14:74067519-74067802 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr14:75277031-75277343 | Common:1; Rare:71 | ||||
chr14:75595937-75596145 | Rare:44 | ||||
chr14:75981889-75982063 | Common:2; Rare:42 | ||||
chr14:76959385-76959636 | Common:1; Rare:43 | ||||
chr14:77026081-77026252 | Rare:55 | ||||
chr14:77027834-77028088 | Rare:101 | ||||
chr14:77032823-77033061 | Common:2; Rare:51 | ||||
chr14:77034047-77034119 | Rare:14 | ||||
chr14:81170371-81170482 | Rare:27 | ||||
chr14:81219345-81219513 | Rare:37 | ||||
chr14:90383215-90383523 | Common:2; Rare:99 | ||||
chr14:92824327-92824590 | Common:5; Rare:64 | ||||
chr14:96039206-96039380 | Common:2; Rare:50 |