Variant report

Variant	rs10782910
Chromosome Location	chr1:103317086-103317087
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10430072	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10735776	0.81[EUR][1000 genomes]
rs10747431	0.81[EUR][1000 genomes]
rs10782909	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10782911	0.89[ASN][1000 genomes]
rs10874660	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10874661	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11164628	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11164629	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11164630	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11164632	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11164633	0.82[EUR][1000 genomes]
rs12023984	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12132471	0.80[EUR][1000 genomes]
rs12133652	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12136992	0.80[EUR][1000 genomes]
rs12144719	0.83[EUR][1000 genomes]
rs12404334	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12406439	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12410008	0.87[EUR][1000 genomes]
rs1241171	0.87[ASN][1000 genomes]
rs1241187	0.87[ASN][1000 genomes]
rs1241196	0.87[ASN][1000 genomes]
rs1241201	0.87[ASN][1000 genomes]
rs1241202	0.87[ASN][1000 genomes]
rs1241206	0.83[ASN][1000 genomes]
rs1241209	0.83[ASN][1000 genomes]
rs1270748	0.87[ASN][1000 genomes]
rs1318755	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1463048	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1599703	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1599706	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1763348	0.86[ASN][1000 genomes]
rs1839632	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1841841	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1932331	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1932341	0.81[EUR][1000 genomes]
rs2077569	0.87[EUR][1000 genomes]
rs2086014	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2169608	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2169609	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2169610	0.83[ASN][1000 genomes]
rs2229783	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2376259	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2616003	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs34689850	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4590689	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4908262	0.81[EUR][1000 genomes]
rs61157885	0.86[ASN][1000 genomes]
rs61812153	0.81[EUR][1000 genomes]
rs644019	0.87[ASN][1000 genomes]
rs7521799	0.81[EUR][1000 genomes]
rs921416	0.81[EUR][1000 genomes]
rs945326	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9787064	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830882	chr1:103192683-103355802	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv522922	chr1:103305021-103764640	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103311200-103319200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103316400-103317400	Enhancers	Placenta	Placenta
3	chr1:103316400-103319400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:103316600-103317200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:103316600-103317200	Enhancers	NH-A	brain
6	chr1:103316600-103318400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:103316600-103319400	Enhancers	Fetal Muscle Leg	muscle
8	chr1:103317000-103317200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:103317000-103318400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:103317000-103318400	Enhancers	Osteobl	bone
11	chr1:103317000-103318600	Enhancers	HSMMtube	muscle

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