Variant report

Variant	rs17103951
Chromosome Location	chr11:105049892-105049893
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10502046	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10502047	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12281540	0.85[EUR][1000 genomes]
rs12416756	0.85[EUR][1000 genomes]
rs12417050	1.00[CEU][hapmap]
rs12417470	1.00[CEU][hapmap]
rs12419220	0.82[EUR][1000 genomes]
rs12420524	0.85[EUR][1000 genomes]
rs12420557	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12420601	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12421544	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12421898	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12796365	0.92[EUR][1000 genomes]
rs12797298	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12797775	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12800151	1.00[CEU][hapmap]
rs12801987	1.00[CEU][hapmap]
rs12806837	0.82[EUR][1000 genomes]
rs1354322	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1503386	0.85[EUR][1000 genomes]
rs1503395	0.92[EUR][1000 genomes]
rs17103670	1.00[CEU][hapmap]
rs17103773	0.89[EUR][1000 genomes]
rs17103781	0.92[EUR][1000 genomes]
rs17103836	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17103858	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17103866	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17103873	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17103953	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17376738	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17377910	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17378343	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2047840	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2047841	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2062807	0.85[EUR][1000 genomes]
rs2062808	0.85[EUR][1000 genomes]
rs2155817	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2409065	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3181328	1.00[CHB][hapmap]
rs34212668	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34255114	0.82[EUR][1000 genomes]
rs35120805	0.90[EUR][1000 genomes]
rs35136587	0.82[EUR][1000 genomes]
rs35394521	0.92[EUR][1000 genomes]
rs35560124	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35565964	0.85[EUR][1000 genomes]
rs35743576	0.85[EUR][1000 genomes]
rs475266	0.89[CEU][hapmap]
rs4754122	0.92[EUR][1000 genomes]
rs4754123	0.92[EUR][1000 genomes]
rs4754124	0.92[EUR][1000 genomes]
rs4754125	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4755076	0.85[EUR][1000 genomes]
rs4755077	0.92[EUR][1000 genomes]
rs4755078	0.92[EUR][1000 genomes]
rs4755079	0.92[EUR][1000 genomes]
rs4755080	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs4755081	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs481926	1.00[CEU][hapmap]
rs486123	1.00[CEU][hapmap]
rs530009	1.00[CEU][hapmap]
rs538943	1.00[CEU][hapmap]
rs567303	0.89[CEU][hapmap]
rs58131087	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60235102	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67835723	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7117758	0.92[EUR][1000 genomes]
rs71484390	0.82[EUR][1000 genomes]
rs71484394	0.85[EUR][1000 genomes]
rs71484399	0.92[EUR][1000 genomes]
rs71484400	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71484401	0.92[EUR][1000 genomes]
rs71484402	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7929852	0.85[EUR][1000 genomes]
rs7930712	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	nsv528789	chr11:105014564-105133046	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1045900	chr11:105015999-105138877	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv556220	chr11:105042650-105112018	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv2762942	chr11:105044258-105066898	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv38978	chr11:105049275-105051786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	nsv442242	chr11:105049805-105066898	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105048600-105050200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr11:105048600-105052000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr11:105048600-105052200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:105048600-105052200	Weak transcription	NHLF	lung
5	chr11:105048600-105052400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:105048600-105052400	Weak transcription	NHDF-Ad	bronchial
7	chr11:105048800-105051800	Weak transcription	NH-A	brain
8	chr11:105049000-105052200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr11:105049200-105052400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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