Variant report

Variant	rs61891101
Chromosome Location	chr11:105001135-105001136
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:105000203..105002774-chr11:105190534..105192628,2	K562	blood:

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1023953	0.97[ASN][1000 genomes]
rs1023954	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10895776	0.99[ASN][1000 genomes]
rs10895778	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10895779	0.87[ASN][1000 genomes]
rs10895780	0.99[ASN][1000 genomes]
rs10895781	0.96[ASN][1000 genomes]
rs10895785	0.85[ASN][1000 genomes]
rs10895787	0.83[ASN][1000 genomes]
rs10895788	0.95[ASN][1000 genomes]
rs10895789	0.95[ASN][1000 genomes]
rs10895790	0.85[ASN][1000 genomes]
rs11226619	0.97[ASN][1000 genomes]
rs11226622	0.87[ASN][1000 genomes]
rs11226624	0.87[ASN][1000 genomes]
rs11226625	0.87[ASN][1000 genomes]
rs11226626	0.87[ASN][1000 genomes]
rs11226627	0.99[ASN][1000 genomes]
rs11226628	0.87[ASN][1000 genomes]
rs11226629	0.99[ASN][1000 genomes]
rs11226630	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11226631	0.87[ASN][1000 genomes]
rs11226633	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11226635	0.87[ASN][1000 genomes]
rs11226641	0.85[ASN][1000 genomes]
rs11226642	0.96[ASN][1000 genomes]
rs11226645	0.85[ASN][1000 genomes]
rs11226649	0.92[ASN][1000 genomes]
rs11226650	0.92[ASN][1000 genomes]
rs11226653	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11226655	0.95[ASN][1000 genomes]
rs11226657	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12222812	0.87[ASN][1000 genomes]
rs12222898	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12226317	0.95[ASN][1000 genomes]
rs1351686	0.93[ASN][1000 genomes]
rs1354319	0.87[ASN][1000 genomes]
rs1354320	0.87[ASN][1000 genomes]
rs1354321	0.87[ASN][1000 genomes]
rs1354323	0.87[ASN][1000 genomes]
rs1393908	0.97[ASN][1000 genomes]
rs1503390	0.97[ASN][1000 genomes]
rs1503392	0.97[ASN][1000 genomes]
rs1503394	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503397	0.87[ASN][1000 genomes]
rs1503398	0.87[ASN][1000 genomes]
rs1503401	0.87[ASN][1000 genomes]
rs1566770	0.97[ASN][1000 genomes]
rs17103763	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1842893	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1842894	0.87[ASN][1000 genomes]
rs1847297	0.87[ASN][1000 genomes]
rs1905257	0.85[ASN][1000 genomes]
rs1994136	0.99[ASN][1000 genomes]
rs2017680	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2089048	0.99[ASN][1000 genomes]
rs2200164	0.94[ASN][1000 genomes]
rs2200165	0.96[ASN][1000 genomes]
rs2200166	0.85[ASN][1000 genomes]
rs2291269	0.99[ASN][1000 genomes]
rs2409063	0.95[ASN][1000 genomes]
rs35868202	0.87[ASN][1000 genomes]
rs3926237	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4754126	0.96[ASN][1000 genomes]
rs4755082	0.87[ASN][1000 genomes]
rs4755083	0.83[ASN][1000 genomes]
rs4755084	0.87[ASN][1000 genomes]
rs4755085	0.87[ASN][1000 genomes]
rs4755086	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4755087	0.99[ASN][1000 genomes]
rs4755088	0.87[ASN][1000 genomes]
rs4755089	0.87[ASN][1000 genomes]
rs4755090	0.87[ASN][1000 genomes]
rs4755091	0.96[ASN][1000 genomes]
rs4755094	0.95[ASN][1000 genomes]
rs4755095	0.94[ASN][1000 genomes]
rs4755096	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5002812	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56180195	0.99[ASN][1000 genomes]
rs57747660	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61891100	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61891102	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61891134	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61891136	0.87[ASN][1000 genomes]
rs6591111	0.99[ASN][1000 genomes]
rs7113151	0.99[ASN][1000 genomes]
rs764078	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7925360	0.87[ASN][1000 genomes]
rs7925579	0.87[ASN][1000 genomes]
rs7934633	0.99[ASN][1000 genomes]
rs7940485	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7943658	0.87[ASN][1000 genomes]
rs7943758	0.87[ASN][1000 genomes]
rs7943776	0.87[ASN][1000 genomes]
rs7943892	0.99[ASN][1000 genomes]
rs7948306	0.87[ASN][1000 genomes]
rs7948428	0.87[ASN][1000 genomes]
rs7952721	0.99[ASN][1000 genomes]
rs995241	0.87[ASN][1000 genomes]
rs995242	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription 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	14 gene(s)	inside rSNPs	diseases
2	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv468862	chr11:104774014-105243371	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
4	nsv556218	chr11:104774014-105243371	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
5	esv3385159	chr11:104786549-105051555	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv1044970	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv541160	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription 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	13 gene(s)	inside rSNPs	diseases
8	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv975866	chr11:104994182-105034480	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

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105000800-105001600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:105000800-105001600	Enhancers	NHEK	skin
3	chr11:105000800-105001800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:105000800-105001800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:105000800-105002000	Enhancers	HMEC	breast
6	chr11:105000800-105002200	Enhancers	Placenta	Placenta
7	chr11:105001000-105001600	Enhancers	Esophagus	oesophagus

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