Variant report

Variant	rs17437679
Chromosome Location	chr4:96305584-96305585
allele	A/C
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]
rs10005976	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs12502414	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs13117954	0.89[CEU][hapmap];0.94[EUR][1000 genomes]
rs17023685	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[YRI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17371089	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1994175	1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34023803	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34959330	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35019760	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs71601273	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[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	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1001955	chr4:96216118-96445841	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96285200-96334600	Weak transcription	Aorta	Aorta
2	chr4:96296400-96316000	Weak transcription	Fetal Kidney	kidney
3	chr4:96299000-96305600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr4:96299000-96310200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr4:96303000-96306400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:96303200-96309600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:96304200-96307400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr4:96304200-96308400	Weak transcription	Brain Angular Gyrus	brain
9	chr4:96304200-96311600	Weak transcription	Brain Substantia Nigra	brain
10	chr4:96304200-96323000	Weak transcription	Brain Anterior Caudate	brain
11	chr4:96304200-96333000	Weak transcription	Fetal Lung	lung
12	chr4:96304600-96306000	Weak transcription	Brain Hippocampus Middle	brain
13	chr4:96305400-96305800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:96305400-96306000	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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