Variant report

Variant	rs6791363
Chromosome Location	chr3:85073170-85073171
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12714616	0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12714617	0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13066623	0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13078384	1.00[CHB][hapmap]
rs13082518	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13092125	0.83[AMR][1000 genomes]
rs13095644	1.00[CHB][hapmap]
rs13096651	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2101344	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs2171143	0.85[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs4516626	1.00[CHB][hapmap]
rs6808586	1.00[CHB][hapmap]
rs7628129	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs7630382	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs9309967	1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9647393	0.88[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9815258	0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9818659	0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9821807	0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9823454	0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9828496	0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9835904	1.00[CHB][hapmap]
rs9838091	1.00[CHB][hapmap]
rs9860513	0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9873321	1.00[CHB][hapmap]
rs9874302	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9876378	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9877460	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9878472	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs9878707	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9881257	0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9883443	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv1829788	chr3:84926769-85086403	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv492289	chr3:85066623-85319147	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85055800-85081400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr3:85065200-85082200	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:85068600-85090600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:85071000-85073400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:85071400-85082400	Weak transcription	Fetal Brain Female	brain
6	chr3:85071600-85074400	Weak transcription	Brain Substantia Nigra	brain
7	chr3:85071600-85082000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr3:85071800-85081400	Weak transcription	Brain Angular Gyrus	brain
9	chr3:85072800-85073600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:85072800-85073800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr3:85073000-85073200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:85073000-85073600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:85073000-85073600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr3:85073000-85074000	Enhancers	HUES6 Cell Line	embryonic stem cell

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