Variant report

Variant	rs7822098
Chromosome Location	chr8:120020129-120020130
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10090576	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10091277	0.80[EUR][1000 genomes]
rs10505348	0.81[CEU][hapmap];0.82[JPT][hapmap]
rs10505351	0.84[EUR][1000 genomes]
rs10955919	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10955924	0.83[EUR][1000 genomes]
rs11573829	0.82[JPT][hapmap]
rs11573885	0.82[JPT][hapmap]
rs11992136	0.91[JPT][hapmap]
rs12682278	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13254554	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13260214	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13262276	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13264791	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1485289	0.82[JPT][hapmap]
rs1872422	0.87[EUR][1000 genomes]
rs1872423	0.83[EUR][1000 genomes]
rs1872426	0.82[JPT][hapmap]
rs1905783	0.85[EUR][1000 genomes]
rs1905784	0.85[EUR][1000 genomes]
rs1905786	0.82[JPT][hapmap]
rs2062375	0.87[CEU][hapmap];0.82[JPT][hapmap]
rs2062377	0.91[CEU][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2073617	0.83[CEU][hapmap]
rs2073618	0.82[JPT][hapmap]
rs2220189	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2450083	0.86[CEU][hapmap]
rs28437165	0.84[EUR][1000 genomes]
rs28621599	0.84[EUR][1000 genomes]
rs3134063	0.82[CEU][hapmap]
rs4242592	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs4273881	0.84[EUR][1000 genomes]
rs4305930	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4307369	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4313185	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4319131	0.82[JPT][hapmap]
rs4335155	0.83[EUR][1000 genomes]
rs4336637	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4354338	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4355805	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4397431	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4403440	0.80[EUR][1000 genomes]
rs4403441	0.85[EUR][1000 genomes]
rs4424291	0.85[EUR][1000 genomes]
rs4424296	0.82[EUR][1000 genomes]
rs4495461	0.82[EUR][1000 genomes]
rs4567065	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4615609	0.84[EUR][1000 genomes]
rs4618726	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4876876	0.91[JPT][hapmap]
rs6415470	0.82[JPT][hapmap]
rs6469789	0.82[JPT][hapmap]
rs6469794	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6469795	0.85[EUR][1000 genomes]
rs6469796	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6469797	0.85[EUR][1000 genomes]
rs6469798	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67819415	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6984287	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6984572	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6993813	0.88[EUR][1000 genomes]
rs6996754	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6999476	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7004052	0.85[EUR][1000 genomes]
rs7006553	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs7010043	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7010267	0.82[JPT][hapmap]
rs7013203	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013722	0.84[EUR][1000 genomes]
rs7016585	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7463176	0.82[JPT][hapmap]
rs7464496	0.82[JPT][hapmap]
rs7813486	0.85[EUR][1000 genomes]
rs7838083	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7842942	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9650075	0.85[EUR][1000 genomes]
rs9969672	0.91[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868916	chr8:119911943-120762250	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758169	chr8:119943309-120275750	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2759639	chr8:119943309-120275750	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv522241	chr8:119995697-120027871	Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
5	nsv437631	chr8:120015963-120051656	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	esv3481077	chr8:120017571-120022669	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3481078	chr8:120017571-120022669	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3517864	chr8:120018471-120028869	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3517862	chr8:120018921-120028769	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv8384	chr8:120019002-120029549	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3517866	chr8:120019189-120029959	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv21198	chr8:120019379-120027798	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3479924	chr8:120019474-120027857	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3517865	chr8:120019500-120027883	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3517867	chr8:120019503-120027862	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3517868	chr8:120019524-120027810	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3479925	chr8:120019528-120027850	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	esv3479926	chr8:120019532-120027843	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3479927	chr8:120019546-120027801	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv3517860	chr8:120019559-120027822	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3517861	chr8:120019580-120027828	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	nsv465788	chr8:120019593-120022486	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	nsv612051	chr8:120019593-120022486	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
24	nsv818654	chr8:120019593-120022486	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3693006	chr8:120019593-120025341	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv2421422	chr8:120019593-120027871	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	nsv515918	chr8:120019593-120029709	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
28	esv3479928	chr8:120019621-120027777	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
29	esv3517869	chr8:120019621-120027777	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120019600-120021000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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