Variant report

Variant	rs763896
Chromosome Location	chr7:28017263-28017264
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11761628	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17695685	0.81[CEU][hapmap]
rs2106922	0.84[CEU][hapmap]
rs2391492	0.81[AMR][1000 genomes]
rs34079332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34714526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36199538	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs38509	0.90[AFR][1000 genomes]
rs3857729	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6956423	1.00[JPT][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes]
rs6966465	0.80[CEU][hapmap];0.85[EUR][1000 genomes]
rs7384844	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs740126	0.92[CEU][hapmap]
rs740127	0.92[CEU][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9648343	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949025	chr7:27578167-28075172	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1030685	chr7:27844038-28177301	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1024819	chr7:27949955-28020969	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:28000600-28019400	Weak transcription	Pancreas	Pancrea
2	chr7:28000600-28021600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:28002800-28034600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:28006200-28019200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:28006200-28024800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:28006400-28031800	Weak transcription	NHDF-Ad	bronchial
7	chr7:28007000-28019200	Weak transcription	Esophagus	oesophagus
8	chr7:28009800-28021600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr7:28012400-28022200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr7:28012400-28028000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr7:28013400-28020000	Strong transcription	Primary B cells from cord blood	blood
12	chr7:28013400-28034200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:28015600-28032400	Weak transcription	Ovary	ovary
14	chr7:28016800-28018000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:28017200-28017600	ZNF genes & repeats	Aorta	Aorta
16	chr7:28017200-28017600	ZNF genes & repeats	Left Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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