Variant report

Variant	rs2081362
Chromosome Location	chr11:57393884-57393885
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10792110	0.89[JPT][hapmap]
rs10896644	1.00[JPT][hapmap]
rs10896649	0.89[JPT][hapmap]
rs11229109	0.89[JPT][hapmap]
rs11570176	1.00[JPT][hapmap]
rs11570181	1.00[JPT][hapmap]
rs1557522	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1613592	1.00[JPT][hapmap]
rs1631684	1.00[JPT][hapmap]
rs1647396	0.92[ASN][1000 genomes]
rs1647403	0.88[JPT][hapmap]
rs17455422	1.00[JPT][hapmap]
rs1783826	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1783827	1.00[JPT][hapmap]
rs1783828	1.00[JPT][hapmap]
rs1783978	1.00[JPT][hapmap]
rs1783979	1.00[JPT][hapmap]
rs1783980	0.89[JPT][hapmap]
rs1783981	0.89[JPT][hapmap]
rs1783983	1.00[JPT][hapmap]
rs1785498	0.88[JPT][hapmap]
rs1798172	1.00[JPT][hapmap]
rs1798173	1.00[JPT][hapmap]
rs1798177	1.00[JPT][hapmap]
rs2156638	0.89[JPT][hapmap]
rs2454660	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2508441	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2508443	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2509897	0.80[CEU][hapmap]
rs2511989	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2511993	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2511994	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2511996	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2926664	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2956981	1.00[JPT][hapmap]
rs3017889	1.00[JPT][hapmap]
rs35196561	0.86[ASN][1000 genomes]
rs36036499	1.00[JPT][hapmap]
rs4611222	0.89[JPT][hapmap]
rs653889	1.00[JPT][hapmap]
rs665058	1.00[JPT][hapmap]
rs7117020	1.00[JPT][hapmap]
rs7120868	1.00[JPT][hapmap]
rs7947357	1.00[JPT][hapmap]
rs929934	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv530621	chr11:57139699-57703639	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	nsv832163	chr11:57299354-57481050	Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv1040913	chr11:57315006-57696122	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2081362	TIMM10	Cis_1M	lymphoblastoid	RTeQTL
rs2081362	TIMM10	cis	Esophagus Muscularis	GTEx
rs2081362	TIMM10	cis	Esophagus Mucosa	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57382200-57395000	Weak transcription	Right Ventricle	heart
2	chr11:57384400-57404800	Weak transcription	Fetal Lung	lung
3	chr11:57387200-57398600	Strong transcription	Liver	Liver
4	chr11:57387600-57397600	Weak transcription	Aorta	Aorta
5	chr11:57387600-57405200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:57389200-57404400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr11:57392400-57394200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:57393600-57401000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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