Variant report

Variant	rs7122887
Chromosome Location	chr11:85292310-85292311
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs1046216	0.91[CHB][hapmap];0.97[CHD][hapmap];0.89[YRI][hapmap];0.84[ASN][1000 genomes]
rs11234359	0.81[CHB][hapmap]
rs11600919	0.84[ASN][1000 genomes]
rs11603256	0.83[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11606688	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11821005	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1213257	0.81[EUR][1000 genomes]
rs1237203	0.95[CHB][hapmap];0.84[CHD][hapmap]
rs1354397	0.81[CHB][hapmap]
rs1425223	0.84[AFR][1000 genomes]
rs1504029	0.88[AFR][1000 genomes]
rs1847433	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2081445	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2196168	0.83[ASW][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap];0.81[LWK][hapmap];0.89[YRI][hapmap]
rs2290823	0.88[ASW][hapmap];0.86[YRI][hapmap]
rs2840343	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs286499	0.81[CHB][hapmap]
rs286511	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs286513	0.81[CHB][hapmap]
rs286515	0.81[CHB][hapmap]
rs290173	0.82[CHB][hapmap]
rs290180	0.82[CHB][hapmap];0.85[CHD][hapmap]
rs290183	0.93[CHB][hapmap];0.86[YRI][hapmap];0.82[ASN][1000 genomes]
rs290184	0.83[ASW][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.86[MKK][hapmap];0.89[YRI][hapmap];0.84[ASN][1000 genomes]
rs290185	0.95[CHB][hapmap];0.92[CHD][hapmap];0.83[YRI][hapmap]
rs290190	0.86[CHB][hapmap]
rs290195	0.86[CHB][hapmap]
rs290200	0.82[CHB][hapmap]
rs290202	0.86[CHB][hapmap]
rs370385	0.95[CHB][hapmap];0.82[YRI][hapmap]
rs3753050	0.83[ASW][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.87[LWK][hapmap];0.86[MKK][hapmap];0.89[YRI][hapmap];0.85[ASN][1000 genomes]
rs3781815	0.92[CEU][hapmap];0.95[CHB][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3817087	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3824956	0.83[ASW][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.81[LWK][hapmap];0.86[MKK][hapmap];0.89[YRI][hapmap];0.85[ASN][1000 genomes]
rs3862782	0.83[ASW][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap];0.85[LWK][hapmap];0.89[YRI][hapmap];0.83[ASN][1000 genomes]
rs4015271	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4301809	0.86[ASN][1000 genomes]
rs431606	0.82[CHB][hapmap];0.82[CHD][hapmap]
rs491867	0.82[CHB][hapmap]
rs4943918	0.81[CHB][hapmap]
rs4943922	0.90[AFR][1000 genomes]
rs4943923	0.90[AFR][1000 genomes]
rs4944523	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4944526	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4944530	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs522604	0.89[ASN][1000 genomes]
rs552013	0.89[ASN][1000 genomes]
rs55739259	0.81[AFR][1000 genomes]
rs55841425	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57245119	0.92[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs57296431	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs575050	0.88[CHD][hapmap]
rs57549298	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs592460	0.95[CHB][hapmap];0.89[ASN][1000 genomes]
rs61114547	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61342895	0.90[ASN][1000 genomes]
rs61567739	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7107788	0.83[ASW][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.87[LWK][hapmap];0.86[MKK][hapmap];0.89[YRI][hapmap];0.85[ASN][1000 genomes]
rs7110363	0.81[CHB][hapmap]
rs7113528	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7116195	0.83[ASW][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap];0.81[LWK][hapmap];0.89[YRI][hapmap];0.81[ASN][1000 genomes]
rs7119617	0.86[YRI][hapmap]
rs7120523	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7925739	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7940714	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7943586	0.88[ASW][hapmap];0.81[LWK][hapmap];0.89[YRI][hapmap]
rs7948778	0.96[YRI][hapmap];0.91[AFR][1000 genomes]
rs7949567	0.81[EUR][1000 genomes]
rs881120	0.95[CHB][hapmap];1.00[CHD][hapmap];0.89[LWK][hapmap];0.93[YRI][hapmap];0.89[ASN][1000 genomes]
rs956202	0.92[CEU][hapmap];0.95[CHB][hapmap];0.82[YRI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv1050363	chr11:85163437-85293233	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv541111	chr11:85163437-85293233	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv898046	chr11:85180409-85300458	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv898047	chr11:85180409-85377707	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
9	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv898048	chr11:85206156-85404138	Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv898049	chr11:85231475-85292310	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85284200-85292400	Weak transcription	Left Ventricle	heart
2	chr11:85284400-85293800	Weak transcription	Ovary	ovary
3	chr11:85287000-85292400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr11:85291400-85299000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr11:85292000-85292400	ZNF genes & repeats	Aorta	Aorta
6	chr11:85292200-85292400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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