Variant report

Variant	rs545735581
Chromosome Location	chr6:70205315-70205316
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432919	chr6:69873179-70221322	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1020330	chr6:70179593-70223307	Active TSS Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
3	nsv1021249	chr6:70186260-70237744	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
4	esv11472	chr6:70188989-70277993	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
5	nsv1020740	chr6:70189036-70223307	ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv432921	chr6:70189506-70221322	ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70205200-70205400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

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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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