Variant report

Variant	rs61893228
Chromosome Location	chr11:104569187-104569188
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10502036	0.90[EUR][1000 genomes]
rs10502037	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10502041	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10791717	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10791719	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10895705	0.83[EUR][1000 genomes]
rs10895706	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10895707	0.87[EUR][1000 genomes]
rs10895708	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10895711	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10895712	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10895713	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10895714	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10895715	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10895719	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10895721	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226426	0.86[EUR][1000 genomes]
rs11226428	0.88[EUR][1000 genomes]
rs11226430	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11226431	0.87[EUR][1000 genomes]
rs11226433	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11226439	0.93[EUR][1000 genomes]
rs11226441	0.93[EUR][1000 genomes]
rs11226442	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11226443	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11226445	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11226448	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11226450	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11226452	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11226456	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11226457	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11226459	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11226460	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11226469	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11226486	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1147010	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147024	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11607612	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1200613	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1200618	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1201816	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12286808	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12361024	0.87[EUR][1000 genomes]
rs12364844	0.93[EUR][1000 genomes]
rs12365448	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12366152	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12418899	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12799900	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12803385	0.87[EUR][1000 genomes]
rs12803710	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1586464	0.86[EUR][1000 genomes]
rs16894	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17102731	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17102776	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1893461	0.90[EUR][1000 genomes]
rs1942502	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1942507	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1942520	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1942521	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2156127	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2187131	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2187132	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2187135	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2226749	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2850817	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34526738	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34793132	0.85[EUR][1000 genomes]
rs55779335	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56384112	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59832858	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61893183	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61893194	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61893229	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7119997	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs722354	0.84[EUR][1000 genomes]
rs7927206	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7935104	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7939905	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9666573	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9667051	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044271	chr11:104136156-104666252	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	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
3	nsv1054456	chr11:104358924-104805251	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	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
5	nsv832254	chr11:104412769-104607277	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2761706	chr11:104523335-104634024	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1050346	chr11:104548749-104664665	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs61893228	CASP1	Cis_1M	lymphoblastoid	RTeQTL
rs61893228	CASP4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104565800-104571000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr11:104565800-104571200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:104566000-104570800	Weak transcription	NHDF-Ad	bronchial
4	chr11:104566000-104571200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:104566200-104571000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:104566200-104571000	Weak transcription	NH-A	brain
7	chr11:104566200-104571200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:104566200-104571200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:104566200-104575000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr11:104566400-104570800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:104566400-104571600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr11:104566400-104575000	Weak transcription	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links