Variant report

Variant	rs62560398
Chromosome Location	chr9:18986931-18986932
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10116465	0.84[ASN][1000 genomes]
rs10116604	0.84[ASN][1000 genomes]
rs10119748	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10122564	0.84[ASN][1000 genomes]
rs10811070	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10811096	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10963851	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10963857	0.84[ASN][1000 genomes]
rs10963858	0.84[ASN][1000 genomes]
rs10963860	0.84[ASN][1000 genomes]
rs10963861	0.84[ASN][1000 genomes]
rs10963868	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10963873	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10963882	0.92[ASN][1000 genomes]
rs10963883	0.92[ASN][1000 genomes]
rs10963886	0.92[ASN][1000 genomes]
rs10963888	1.00[ASN][1000 genomes]
rs10963889	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10963890	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11496354	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12115446	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16937210	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17236157	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2039007	0.84[ASN][1000 genomes]
rs2039009	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2233800	0.85[EUR][1000 genomes]
rs28689789	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28742005	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28805064	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3177673	0.85[EUR][1000 genomes]
rs4478656	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62560397	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62560399	1.00[EUR][1000 genomes]
rs62560432	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62560442	0.84[EUR][1000 genomes]
rs7873306	0.85[ASN][1000 genomes]
rs883440	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9657571	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[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	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv949111	chr9:18758205-18994588	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv1017820	chr9:18882219-19587377	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
7	nsv540078	chr9:18882219-19587377	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
8	nsv892699	chr9:18945868-19025693	Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1022697	chr9:18951530-19010894	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv892700	chr9:18979441-19156784	Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18984400-18987800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr9:18984800-18988200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:18985800-18987400	Enhancers	Fetal Kidney	kidney
4	chr9:18985800-18991800	Weak transcription	Pancreas	Pancrea
5	chr9:18985800-18993400	Weak transcription	Fetal Thymus	thymus

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