Variant report

Variant	rs11606688
Chromosome Location	chr11:85318520-85318521
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:85317935..85319449-chr11:85332481..85334834,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1046216	0.91[CHB][hapmap];0.95[CHD][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10501595	0.93[YRI][hapmap]
rs11234359	0.81[CHB][hapmap]
rs11600919	0.88[ASN][1000 genomes]
rs11603256	0.92[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11821005	0.84[ASN][1000 genomes]
rs1192	0.88[LWK][hapmap];0.87[YRI][hapmap]
rs1214001	0.80[LWK][hapmap];0.93[YRI][hapmap]
rs1237203	0.95[CHB][hapmap];0.81[CHD][hapmap]
rs12419172	0.89[ASW][hapmap];0.88[LWK][hapmap];0.93[YRI][hapmap]
rs1354397	0.81[CHB][hapmap]
rs2117312	0.80[ASN][1000 genomes]
rs2196168	0.95[CHB][hapmap];0.84[CHD][hapmap];0.82[ASN][1000 genomes]
rs2840343	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs286499	0.81[CHB][hapmap]
rs286513	0.81[CHB][hapmap]
rs286515	0.81[CHB][hapmap]
rs290173	0.82[CHB][hapmap]
rs290180	0.82[CHB][hapmap];0.82[CHD][hapmap]
rs290181	0.80[ASN][1000 genomes]
rs290182	0.93[YRI][hapmap]
rs290183	0.93[CHB][hapmap];0.86[ASN][1000 genomes]
rs290184	0.95[CHB][hapmap];0.90[CHD][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs290185	0.95[CHB][hapmap];0.89[CHD][hapmap];0.80[ASN][1000 genomes]
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];0.81[ASN][1000 genomes]
rs3753050	0.95[CHB][hapmap];0.90[CHD][hapmap];0.89[ASN][1000 genomes]
rs3781815	0.92[CEU][hapmap];0.95[CHB][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3817087	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3824956	0.95[CHB][hapmap];0.90[CHD][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3862782	0.95[CHB][hapmap];0.84[CHD][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4015271	0.87[ASN][1000 genomes]
rs4301809	0.82[ASN][1000 genomes]
rs431606	0.82[CHB][hapmap]
rs491867	0.82[CHB][hapmap]
rs4943918	0.81[CHB][hapmap]
rs4944523	0.80[EUR][1000 genomes]
rs4944526	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4944530	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs522604	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs552013	0.94[ASN][1000 genomes]
rs57245119	0.83[ASN][1000 genomes]
rs57296431	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs575050	0.85[CHD][hapmap]
rs57549298	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs592460	0.95[CHB][hapmap];0.94[ASN][1000 genomes]
rs61114547	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61342895	0.86[ASN][1000 genomes]
rs61567739	0.85[EUR][1000 genomes]
rs6592252	0.80[AFR][1000 genomes]
rs6592253	0.83[AFR][1000 genomes]
rs7107788	0.95[CHB][hapmap];0.90[CHD][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7110363	0.81[CHB][hapmap]
rs7113528	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7116195	0.95[CHB][hapmap];0.84[CHD][hapmap];0.86[ASN][1000 genomes]
rs7120523	0.84[ASN][1000 genomes]
rs7122887	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7925739	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7940714	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs881120	0.95[CHB][hapmap];0.97[CHD][hapmap];0.94[ASN][1000 genomes]
rs947863	1.00[ASW][hapmap];0.88[LWK][hapmap];0.93[YRI][hapmap]
rs956202	0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85316200-85319800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr11:85316400-85319200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr11:85317800-85337600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:85318400-85318800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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