Variant report

Variant	rs10095501
Chromosome Location	chr8:79357396-79357397
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10091249	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10095086	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10099720	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10102189	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10107528	0.96[EUR][1000 genomes]
rs10216378	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10282748	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11987891	0.81[JPT][hapmap]
rs11992010	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11993013	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11996494	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13340636	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13438796	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13438972	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16905657	0.81[JPT][hapmap]
rs16905662	0.81[JPT][hapmap]
rs28410079	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28550609	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28718988	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35487809	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4307332	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4421343	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4498528	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55759929	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57065240	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58824115	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59700637	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59894646	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6473105	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72622866	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72622867	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72622868	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72622869	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72622874	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72622880	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72622881	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7817739	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7818554	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7828090	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7833623	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7833709	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9298313	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891056	chr8:79206819-79394667	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1017218	chr8:79287819-79434844	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv539652	chr8:79287819-79434844	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1033453	chr8:79320533-79485680	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv891057	chr8:79340828-79394667	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:79356600-79358000	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr8:79356600-79358000	Active TSS	Primary T cells from cord blood	blood
3	chr8:79356600-79358000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr8:79356800-79357400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr8:79356800-79357400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
6	chr8:79356800-79357800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
7	chr8:79356800-79357800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
8	chr8:79356800-79358000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
9	chr8:79357000-79357400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:79357000-79357400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr8:79357000-79357400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
12	chr8:79357000-79357600	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr8:79357000-79357600	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr8:79357000-79357600	Active TSS	Primary T helper naive cells from peripheral blood	blood
15	chr8:79357000-79357600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:79357000-79357600	Active TSS	Hela-S3	cervix
17	chr8:79357000-79357800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:79357000-79357800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:79357000-79357800	Active TSS	Primary T cells fromperipheralblood	blood
20	chr8:79357000-79357800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr8:79357000-79357800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
22	chr8:79357000-79358000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:79357000-79358000	Enhancers	Fetal Thymus	thymus
24	chr8:79357200-79357400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:79357200-79357400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr8:79357200-79357400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr8:79357200-79357600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:79357200-79357600	Active TSS	H9 Cell Line	embryonic stem cell
29	chr8:79357200-79357600	Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr8:79357200-79357600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:79357200-79357600	Enhancers	Placenta	Placenta
32	chr8:79357200-79357600	Active TSS	Fetal Stomach	stomach
33	chr8:79357200-79358000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:79357200-79358200	Active TSS	Primary T helper cells PMA-I stimulated	--

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