Variant report

Variant	rs35612961
Chromosome Location	chr8:89592275-89592276
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10504857	0.98[ASN][1000 genomes]
rs10504859	0.84[ASN][1000 genomes]
rs11995572	0.87[ASN][1000 genomes]
rs13256903	0.95[ASN][1000 genomes]
rs13267565	0.85[ASN][1000 genomes]
rs13268482	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs13271846	0.84[ASN][1000 genomes]
rs16884251	0.84[ASN][1000 genomes]
rs16884273	0.84[ASN][1000 genomes]
rs16884286	0.84[ASN][1000 genomes]
rs16884288	0.84[ASN][1000 genomes]
rs16884476	0.98[ASN][1000 genomes]
rs2129780	0.84[ASN][1000 genomes]
rs34246550	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs34587669	0.95[ASN][1000 genomes]
rs34846572	0.84[ASN][1000 genomes]
rs34976712	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs35367857	0.84[ASN][1000 genomes]
rs35380858	0.98[ASN][1000 genomes]
rs35672725	0.98[ASN][1000 genomes]
rs35715471	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs35768850	0.84[ASN][1000 genomes]
rs35871366	0.85[ASN][1000 genomes]
rs36025043	0.85[ASN][1000 genomes]
rs36053186	0.83[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4295707	0.83[ASN][1000 genomes]
rs4425798	0.84[ASN][1000 genomes]
rs56945692	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs57236056	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57251672	0.98[ASN][1000 genomes]
rs57311533	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs57772961	0.98[ASN][1000 genomes]
rs58035549	0.84[ASN][1000 genomes]
rs58163231	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs60622165	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs60911627	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66766214	0.85[ASN][1000 genomes]
rs67264423	0.85[ASN][1000 genomes]
rs67865942	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7003288	0.83[ASN][1000 genomes]
rs71526948	0.84[ASN][1000 genomes]
rs71526949	0.98[ASN][1000 genomes]
rs71526953	0.98[ASN][1000 genomes]
rs73692426	0.84[ASN][1000 genomes]
rs7814649	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7817740	0.85[ASN][1000 genomes]
rs7818525	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7819570	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7820262	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7829835	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7833159	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7833613	0.98[ASN][1000 genomes]
rs7837032	0.84[AFR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7838490	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1030028	chr8:89060085-89733470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv891172	chr8:89439469-89640705	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv891173	chr8:89509223-89996790	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1024633	chr8:89517079-89959574	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv539666	chr8:89517079-89959574	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1027744	chr8:89526571-89609651	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv429927	chr8:89529845-89609684	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv520279	chr8:89534091-89607437	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1023877	chr8:89552013-89900874	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv891174	chr8:89578032-89658050	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	esv1010810	chr8:89592267-89593190	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89587000-89596600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr8:89587000-89596600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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