Variant report

Variant	rs7771247
Chromosome Location	chr6:2005591-2005592
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:2005493..2008020-chr6:2019551..2022122,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11242731	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs12206139	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12212324	1.00[CEU][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13218855	0.94[EUR][1000 genomes]
rs1802	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2076916	0.91[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2875725	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4959164	0.90[CEU][hapmap];0.92[EUR][1000 genomes]
rs4959620	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs4959629	0.88[EUR][1000 genomes]
rs4959632	0.81[CEU][hapmap]
rs501038	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs635234	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs6596868	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs668674	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs6909371	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6910252	1.00[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6922565	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6938640	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs7751738	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772545	0.87[JPT][hapmap]
rs9328080	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9378669	0.97[EUR][1000 genomes]
rs9391942	0.87[CEU][hapmap];0.91[EUR][1000 genomes]
rs9392351	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9392366	0.83[CEU][hapmap];0.92[CHB][hapmap]
rs9405537	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9405545	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs9503076	0.91[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes]
rs9503080	0.91[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530548	chr6:1441421-2351608	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv869043	chr6:1744238-2006788	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv931941	chr6:1768439-2246781	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
5	nsv1032149	chr6:1848148-2006021	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1032727	chr6:1900622-2064690	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv538095	chr6:1900622-2064690	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv883386	chr6:1910108-2122454	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv2763525	chr6:1994892-2006033	Enhancers Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:1985000-2010200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:1988400-2008600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:1990200-2008600	Weak transcription	Pancreas	Pancrea
4	chr6:1990400-2010800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:1992800-2010200	Weak transcription	Fetal Intestine Small	intestine
6	chr6:1993000-2021200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:1993200-2007200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr6:2000000-2021200	Weak transcription	Small Intestine	intestine
9	chr6:2001000-2009600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:2002600-2008600	Weak transcription	Gastric	stomach
11	chr6:2002800-2008800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:2005400-2006200	Genic enhancers	HepG2	liver

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