Variant report

Variant	rs62377808
Chromosome Location	chr5:120033970-120033971
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10434768	0.83[ASN][1000 genomes]
rs10434769	0.83[ASN][1000 genomes]
rs10463728	0.86[ASN][1000 genomes]
rs10463729	0.86[ASN][1000 genomes]
rs10519647	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10519648	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1449144	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1449145	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17429630	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17501753	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17501872	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17501927	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1839246	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2122190	0.86[ASN][1000 genomes]
rs2405964	0.83[ASN][1000 genomes]
rs4895272	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4895273	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4895274	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4895275	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59166325	0.83[ASN][1000 genomes]
rs60807869	0.83[ASN][1000 genomes]
rs62377807	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62377810	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62377815	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62377816	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62377818	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62377819	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62379788	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62379789	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6871826	0.83[ASN][1000 genomes]
rs72781609	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72794307	0.86[ASN][1000 genomes]
rs72794308	0.81[ASN][1000 genomes]
rs72794324	0.83[ASN][1000 genomes]
rs72794327	0.83[ASN][1000 genomes]
rs72794329	0.83[ASN][1000 genomes]
rs72794336	0.83[ASN][1000 genomes]
rs72794341	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72794345	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72794351	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72798425	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7736461	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031453	chr5:119843593-120393038	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS 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	9 gene(s)	inside rSNPs	diseases
3	nsv830464	chr5:119950090-120106717	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv599603	chr5:119953529-120317035	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv949415	chr5:119957645-120459183	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv830465	chr5:119973839-120151853	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1030613	chr5:119980213-120301205	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1029773	chr5:120018166-120213999	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1016516	chr5:120023417-120132790	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1022693	chr5:120026332-120132790	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120021200-120037600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:120027800-120035600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:120031400-120034800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:120032800-120034200	Active TSS	H1 Cell Line	embryonic stem cell
5	chr5:120033000-120037600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:120033200-120034000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr5:120033200-120034000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:120033200-120035000	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr5:120033200-120035000	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr5:120033400-120034000	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr5:120033400-120039200	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr5:120033600-120035000	Active TSS	H9 Cell Line	embryonic stem cell
13	chr5:120033800-120034200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr5:120033800-120034200	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell

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