Variant report

Variant	rs1885161
Chromosome Location	chr14:97384491-97384492
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10132650	0.81[EUR][1000 genomes]
rs10138598	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs10143496	0.81[EUR][1000 genomes]
rs10146186	0.81[EUR][1000 genomes]
rs10148005	0.87[CEU][hapmap]
rs10148863	1.00[CEU][hapmap]
rs10148869	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs13379109	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17094675	0.87[ASN][1000 genomes]
rs17094692	0.88[ASN][1000 genomes]
rs17094776	0.83[ASN][1000 genomes]
rs17094780	0.83[ASN][1000 genomes]
rs1884064	0.88[ASN][1000 genomes]
rs2369902	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs28567991	0.81[EUR][1000 genomes]
rs28582851	0.81[EUR][1000 genomes]
rs28587799	0.81[EUR][1000 genomes]
rs28635274	0.81[EUR][1000 genomes]
rs28640027	0.81[EUR][1000 genomes]
rs28667199	0.81[EUR][1000 genomes]
rs57221296	0.91[EUR][1000 genomes]
rs58143547	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs74076183	0.93[EUR][1000 genomes]
rs74076190	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74076844	0.83[ASN][1000 genomes]
rs74078732	0.91[ASN][1000 genomes]
rs8019781	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs863086	0.80[ASN][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	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97368600-97391400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:97376800-97387600	Weak transcription	Thymus	Thymus
3	chr14:97379000-97387800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:97379400-97411800	Weak transcription	Primary T cells from cord blood	blood
5	chr14:97381200-97386200	Weak transcription	Adipose Nuclei	Adipose
6	chr14:97381400-97386400	Weak transcription	Fetal Brain Female	brain
7	chr14:97381400-97386600	Weak transcription	Dnd41	blood
8	chr14:97383200-97387000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr14:97383600-97384600	Enhancers	Fetal Muscle Leg	muscle
10	chr14:97383600-97384600	Flanking Active TSS	K562	blood
11	chr14:97383800-97384600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:97384200-97387000	Weak transcription	Fetal Brain Male	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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