Variant report

Variant	rs6781359
Chromosome Location	chr3:115837531-115837532
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10212348	1.00[EUR][1000 genomes]
rs10212349	1.00[EUR][1000 genomes]
rs10212350	1.00[EUR][1000 genomes]
rs10212351	1.00[EUR][1000 genomes]
rs11914439	1.00[EUR][1000 genomes]
rs11925181	1.00[EUR][1000 genomes]
rs11927187	1.00[EUR][1000 genomes]
rs13067904	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13324181	1.00[EUR][1000 genomes]
rs1381071	1.00[EUR][1000 genomes]
rs1563936	1.00[EUR][1000 genomes]
rs1563939	1.00[EUR][1000 genomes]
rs16824706	1.00[EUR][1000 genomes]
rs1882011	1.00[EUR][1000 genomes]
rs1920361	1.00[EUR][1000 genomes]
rs28410403	1.00[EUR][1000 genomes]
rs35319164	1.00[EUR][1000 genomes]
rs4277686	1.00[EUR][1000 genomes]
rs59092560	1.00[EUR][1000 genomes]
rs59700272	1.00[EUR][1000 genomes]
rs6438298	1.00[EUR][1000 genomes]
rs6768516	1.00[EUR][1000 genomes]
rs6791561	1.00[EUR][1000 genomes]
rs6796602	1.00[EUR][1000 genomes]
rs72947992	1.00[EUR][1000 genomes]
rs72959750	1.00[EUR][1000 genomes]
rs72959752	1.00[EUR][1000 genomes]
rs9283565	1.00[EUR][1000 genomes]
rs9289043	1.00[EUR][1000 genomes]
rs9289044	1.00[EUR][1000 genomes]
rs9818490	1.00[EUR][1000 genomes]
rs9830788	1.00[EUR][1000 genomes]
rs9835051	1.00[EUR][1000 genomes]
rs9856732	1.00[EUR][1000 genomes]

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	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2755046	chr3:115818840-115942952	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv591345	chr3:115819376-115902901	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2752728	chr3:115833212-115902901	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115834800-115844200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:115836800-115838400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:115837000-115838000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:115837000-115838200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:115837000-115838200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:115837000-115838200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:115837000-115838400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:115837200-115837600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr3:115837200-115837600	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr3:115837200-115837600	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr3:115837200-115838200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:115837400-115837600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:115837400-115838000	Enhancers	H1 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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