Variant report

Variant	rs4681327
Chromosome Location	chr3:146219740-146219741
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:146219569..146222344-chr3:146250325..146252358,2	K562	blood:
2	chr3:146210468..146212270-chr3:146218804..146221427,2	MCF-7	breast:
3	chr3:146216120..146218147-chr3:146219212..146221539,2	K562	blood:
4	chr3:146214293..146216886-chr3:146219168..146220915,2	MCF-7	breast:
5	chr3:146219517..146222555-chr3:146227614..146231140,3	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11708619	0.81[EUR][1000 genomes]
rs13068178	0.86[YRI][hapmap]
rs13090489	0.86[YRI][hapmap]
rs1720242	0.81[CEU][hapmap];0.87[TSI][hapmap]
rs2120384	0.85[CEU][hapmap]
rs35296568	0.81[CEU][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs3732746	1.00[CEU][hapmap]
rs4355250	0.86[YRI][hapmap]
rs4572737	0.86[YRI][hapmap]
rs4681119	0.86[YRI][hapmap]
rs473794	0.88[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs474803	0.90[EUR][1000 genomes]
rs487578	0.81[CEU][hapmap];0.84[TSI][hapmap]
rs488053	0.91[EUR][1000 genomes]
rs491900	0.85[CEU][hapmap]
rs506974	0.87[TSI][hapmap];0.92[EUR][1000 genomes]
rs512259	0.91[ASN][1000 genomes]
rs523849	0.81[CEU][hapmap];0.92[EUR][1000 genomes]
rs524720	0.81[CEU][hapmap];0.91[EUR][1000 genomes]
rs527708	0.92[EUR][1000 genomes]
rs533625	0.90[EUR][1000 genomes]
rs534092	0.90[EUR][1000 genomes]
rs536619	0.90[EUR][1000 genomes]
rs536737	0.80[CEU][hapmap]
rs544178	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs546430	0.90[EUR][1000 genomes]
rs557809	0.90[EUR][1000 genomes]
rs563385	0.81[CEU][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs568302	0.85[CEU][hapmap];0.80[JPT][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes]
rs575834	0.81[CEU][hapmap];0.87[TSI][hapmap];0.92[EUR][1000 genomes]
rs577842	0.81[CEU][hapmap];0.94[LWK][hapmap];0.97[MKK][hapmap];0.89[TSI][hapmap];0.93[YRI][hapmap]
rs968634	0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs968635	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877622	chr3:146131961-146219740	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3448053	chr3:146186791-146262066	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	esv3523751	chr3:146186838-146261806	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	esv3523753	chr3:146186838-146261806	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	esv2496437	chr3:146186902-146262961	Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	esv3416587	chr3:146191303-146222138	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4681327	GPR87	cis	cerebellum	SCAN

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146211400-146221200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr3:146214200-146235400	Weak transcription	Right Atrium	heart
3	chr3:146214800-146220600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr3:146215000-146220400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:146215000-146220800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:146216000-146221800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:146216000-146232800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:146216200-146221600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr3:146216200-146224000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr3:146216200-146230000	Weak transcription	Primary B cells from cord blood	blood
11	chr3:146216400-146220600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:146216600-146230200	Weak transcription	Primary T cells from cord blood	blood
13	chr3:146217600-146220200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr3:146217800-146220400	Weak transcription	A549	lung
15	chr3:146218000-146221000	Weak transcription	Fetal Intestine Small	intestine
16	chr3:146218400-146232200	Weak transcription	Aorta	Aorta
17	chr3:146219600-146220400	Enhancers	GM12878-XiMat	blood

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