Variant report

Variant	rs35150383
Chromosome Location	chr8:67290527-67290528
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10093516	0.85[ASN][1000 genomes]
rs10435613	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10435614	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10957373	0.84[ASN][1000 genomes]
rs11784121	0.95[ASN][1000 genomes]
rs12541243	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12674507	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13259712	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13263790	0.85[EUR][1000 genomes]
rs13274386	0.90[EUR][1000 genomes]
rs13278628	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13282925	0.99[ASN][1000 genomes]
rs2555580	0.85[ASN][1000 genomes]
rs28532882	0.86[ASN][1000 genomes]
rs34469344	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34556813	0.90[ASN][1000 genomes]
rs35403851	1.00[EUR][1000 genomes]
rs35502468	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35769205	0.90[ASN][1000 genomes]
rs35929661	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3739336	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6472275	0.90[ASN][1000 genomes]
rs66815352	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6991180	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8180970	0.90[AMR][1000 genomes];1.00[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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3414665	chr8:66936816-67381935	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67288800-67291000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:67289000-67295000	Weak transcription	Placenta	Placenta
3	chr8:67290000-67291200	Enhancers	Brain Germinal Matrix	brain
4	chr8:67290000-67291400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:67290200-67291400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:67290200-67295800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:67290400-67290600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:67290400-67291000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:67290400-67291000	Enhancers	Fetal Brain Female	brain
10	chr8:67290400-67291200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:67290400-67291200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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