Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:60724084-60724471 | Common:1; Rare:111 | ||||
chr14:60980980-60981305 | Common:1; Rare:125 | ||||
chr14:61281183-61281598 | Common:4; Rare:96 | ||||
chr14:61695205-61695586 | Common:3; Rare:118 | ||||
chr14:61762220-61762528 | Common:3; Rare:138 | ||||
chr14:63543289-63543541 | Common:3; Rare:69 | ||||
chr14:63641468-63641591 | Rare:28 | ||||
chr14:63641779-63642171 | Common:6; Rare:123 | ||||
chr14:63727997-63728114 | Common:1; Rare:50 | ||||
chr14:63852880-63853079 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
chr14:64338111-64338374 | Common:2; Rare:54 | ||||
chr14:64387930-64388069 | Rare:27 | ||||
chr14:64388186-64388497 | Common:2; Rare:141 | ||||
chr14:64431587-64431860 | Common:2; Rare:72 | ||||
chr14:64465329-64465595 | Common:1; Rare:74 |