Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633787-49634084 | Common:1; Rare:107; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr14:49775203-49775303 | Rare:20 | ||||
chr14:49789221-49789429 | Rare:56 | ||||
chr14:49789497-49789730 | Rare:52 | ||||
chr14:49853796-49853928 | Rare:30 | ||||
chr14:49862635-49863039 | Common:1; Rare:183 | ||||
chr14:49868129-49868471 | Common:3; Rare:77 | ||||
chr14:49972245-49972522 | Common:3; Rare:50 | ||||
chr14:50000912-50000960 | Rare:13 | ||||
chr14:50001250-50001416 | Common:2; Rare:33 | ||||
chr14:50003413-50003596 | Rare:54 | ||||
chr14:50459840-50460197 | Common:1; Rare:62 | ||||
chr14:52315418-52315617 | Rare:36 | ||||
chr14:55103179-55103558 | Common:1; Rare:81 | ||||
chr14:55125505-55125642 | Common:1; Rare:27 |