Variant report

Variant	rs566880431
Chromosome Location	chr7:61054353-61054354
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv981488	chr7:61054332-61056731	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
2	nsv966805	chr7:61054332-61057367	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:61054200-61055800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
2	chr7:61054200-61055800	ZNF genes & repeats	Liver	Liver
3	chr7:61054200-61055800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr7:61054200-61056000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:61054200-61056000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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