Variant report

Variant	rs4737071
Chromosome Location	chr8:42650436-42650437
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10087172	0.83[JPT][hapmap];0.83[AMR][1000 genomes]
rs10092346	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10105699	0.90[ASN][1000 genomes]
rs10107450	0.90[AMR][1000 genomes]
rs10108797	0.82[AMR][1000 genomes]
rs10109040	0.90[JPT][hapmap];0.83[AMR][1000 genomes]
rs10109429	0.83[JPT][hapmap]
rs10110332	0.84[AMR][1000 genomes]
rs1072003	0.83[JPT][hapmap];0.82[AMR][1000 genomes]
rs11986893	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11995030	0.83[AMR][1000 genomes]
rs1625050	0.86[CHB][hapmap]
rs1960346	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2082591	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2117225	0.83[AMR][1000 genomes]
rs2196128	0.83[JPT][hapmap];0.82[AMR][1000 genomes]
rs2217732	0.83[JPT][hapmap];0.81[AMR][1000 genomes]
rs2304297	0.89[CEU][hapmap];0.83[JPT][hapmap]
rs28501554	0.82[AMR][1000 genomes]
rs28784665	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28826992	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34996273	0.95[ASN][1000 genomes]
rs4509313	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4567031	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4737068	0.83[AMR][1000 genomes]
rs56395510	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6474418	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6474420	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6984252	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6999449	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7000412	0.81[AMR][1000 genomes]
rs7001753	0.81[AMR][1000 genomes]
rs7003968	0.92[ASN][1000 genomes]
rs7005126	0.94[ASN][1000 genomes]
rs773069	0.86[CHB][hapmap]
rs773070	0.84[CHB][hapmap]
rs773072	0.86[CHB][hapmap]
rs7812298	0.83[JPT][hapmap]
rs7825261	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7826201	0.89[ASN][1000 genomes]
rs7831096	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7835435	0.86[CHB][hapmap]
rs7841834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7845365	0.92[ASN][1000 genomes]
rs7845663	0.83[JPT][hapmap]
rs892413	0.83[JPT][hapmap];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530880	chr8:41895241-42755506	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1034724	chr8:42386707-42772203	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	nsv428516	chr8:42577171-42731235	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
4	nsv890846	chr8:42625663-43240123	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:42642200-42651800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:42644800-42650600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:42645600-42651800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr8:42645800-42650800	Enhancers	Primary T cells from cord blood	blood
5	chr8:42645800-42650800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr8:42645800-42658600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr8:42647800-42660200	Weak transcription	Right Atrium	heart
8	chr8:42648400-42650800	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr8:42648600-42650600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr8:42649200-42650600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:42649400-42651600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr8:42649400-42651800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr8:42649600-42651200	Weak transcription	K562	blood
14	chr8:42649600-42651800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr8:42649600-42651800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr8:42650000-42650800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr8:42650000-42650800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr8:42650200-42651400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:42650200-42651800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr8:42650400-42650600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:42650400-42652000	Weak transcription	Fetal Thymus	thymus

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