Variant report

Variant	rs11265584
Chromosome Location	chr1:161261041-161261042
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10494348	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10494349	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12091289	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12093075	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12098224	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12744346	0.92[EUR][1000 genomes]
rs16832738	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs17398501	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs34362626	0.95[EUR][1000 genomes]
rs4477295	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530077	chr1:160836448-161284904	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv432986	chr1:161221133-161673682	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161243000-161261200	Weak transcription	Brain Substantia Nigra	brain
2	chr1:161243200-161264000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:161250400-161274200	Weak transcription	Fetal Stomach	stomach
4	chr1:161252400-161274800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:161254400-161261200	Weak transcription	Brain Anterior Caudate	brain
6	chr1:161255200-161274800	Weak transcription	Lung	lung
7	chr1:161255600-161261200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:161255600-161274600	Weak transcription	Adipose Nuclei	Adipose
9	chr1:161255800-161261200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr1:161256400-161272800	Weak transcription	Primary T cells from cord blood	blood
11	chr1:161259000-161267400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:161260200-161265600	Weak transcription	HepG2	liver
13	chr1:161260400-161261400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr1:161260600-161261800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:161260800-161261400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:161261000-161261400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:161261000-161261400	Enhancers	Fetal Intestine Small	intestine
18	chr1:161261000-161261600	Enhancers	Fetal Intestine Large	intestine
19	chr1:161261000-161272800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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

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