Variant report

Variant	rs1843789
Chromosome Location	chr8:122370480-122370481
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10094084	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10102395	0.83[ASN][1000 genomes]
rs10107573	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10481070	0.83[ASN][1000 genomes]
rs10481147	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10956033	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10956035	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10956038	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10956039	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10956040	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12545486	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13265234	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13265478	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13274258	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1487162	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1487168	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1487169	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1487170	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1565035	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16892957	0.89[ASN][1000 genomes]
rs1843790	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906216	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2046570	0.85[ASN][1000 genomes]
rs2385927	0.83[ASN][1000 genomes]
rs2386122	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2891939	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4144692	0.85[ASN][1000 genomes]
rs4460379	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6469998	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6470000	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6985415	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6988724	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7000174	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7004666	0.89[ASN][1000 genomes]
rs7006642	0.83[ASN][1000 genomes]
rs7006650	0.82[ASN][1000 genomes]
rs7008446	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7008769	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7015873	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7017097	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7824421	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7824450	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7829217	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7838314	0.83[AMR][1000 genomes];0.92[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	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3330574	chr8:122039099-122386130	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv891426	chr8:122078334-122393258	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1025365	chr8:122323246-122394774	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv465792	chr8:122329373-122398867	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv612131	chr8:122329373-122398867	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv831445	chr8:122336877-122509300	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122366800-122371000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:122368000-122370600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:122369800-122372000	Enhancers	NHDF-Ad	bronchial
4	chr8:122370000-122371200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:122370000-122374200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr8:122370200-122371600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:122370400-122370800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:122370400-122374200	Weak transcription	Osteobl	bone

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