Variant report

Variant	rs564020275
Chromosome Location	chr6:35104015-35104016
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3441631	chr6:35103524-35106522	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv511879	chr6:35103668-35106088	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3364376	chr6:35103875-35105623	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2633690	chr6:35103902-35106024	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35103600-35104200	Enhancers	GM12878-XiMat	blood
2	chr6:35103800-35104200	Enhancers	Primary B cells from peripheral blood	blood
3	chr6:35103800-35104200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:35104000-35104200	Enhancers	Adipose Nuclei	Adipose
5	chr6:35104000-35104200	Enhancers	Fetal Lung	lung
6	chr6:35104000-35108600	Weak transcription	Ovary	ovary

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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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