Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100065274-100065473 | Rare:35 | ||||
chr14:100066438-100066492 | Common:1; Rare:15 | ||||
chr14:100238582-100238841 | Common:2; Rare:76 | ||||
chr14:100375287-100375755 | Common:4; Rare:79 | ||||
chr14:100376259-100376511 | Common:3; Rare:80 | ||||
chr14:101809736-101810034 | Rare:71 | ||||
chr14:101810259-101810429 | Common:2; Rare:37 | ||||
chr14:101823765-101824056 | Common:1; Rare:57 | ||||
chr14:101964463-101964704 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
chr14:102086984-102087357 | Common:5; Rare:157 | ||||
chr14:102139650-102139923 | Rare:95 | ||||
chr14:102362836-102363094 | Rare:118 | ||||
chr14:102592350-102592658 | Common:1; Rare:125 | ||||
chr14:102928532-102928679 | Rare:47 | ||||
chr14:103123264-103123481 | Rare:38 |