Variant report

Variant	rs10036203
Chromosome Location	chr5:108446522-108446523
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:108441092..108442647-chr5:108444693..108446908,2	MCF-7	breast:

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10035284	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10040665	0.84[CEU][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10051034	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10055161	0.80[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10056059	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10063768	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10066375	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10067445	0.87[ASN][1000 genomes]
rs10069467	1.00[JPT][hapmap];0.80[YRI][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10074150	0.80[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10074425	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10076453	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10080132	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10213898	0.87[ASN][1000 genomes]
rs10214383	0.87[ASN][1000 genomes]
rs10214384	0.87[ASN][1000 genomes]
rs1036214	0.84[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10477438	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10477439	1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10477951	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10477955	0.85[ASN][1000 genomes]
rs10900651	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11746231	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11749629	1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11750370	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11952637	0.80[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11957989	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12332736	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17161607	0.85[AMR][1000 genomes]
rs17161612	0.84[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17407717	1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17450338	0.87[CEU][hapmap]
rs17450490	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28433735	0.85[AMR][1000 genomes]
rs28759518	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3797838	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3797843	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3797845	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3814065	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4130644	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs4957568	0.86[ASN][1000 genomes]
rs4957569	0.80[CEU][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4957797	0.96[CEU][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55699307	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67436896	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6861626	0.85[ASN][1000 genomes]
rs6865568	0.91[CEU][hapmap]
rs6869357	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6873546	0.80[CEU][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6882003	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6882531	1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6883750	0.87[ASN][1000 genomes]
rs6894117	0.83[AMR][1000 genomes]
rs6896724	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72796568	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72796593	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72796595	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72796596	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72798574	0.83[ASN][1000 genomes]
rs72798576	0.82[ASN][1000 genomes]
rs7709466	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7709482	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7724901	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7731193	0.96[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735111	0.85[JPT][hapmap]
rs7736773	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9285864	0.85[JPT][hapmap]
rs9326763	0.84[ASN][1000 genomes]
rs9326764	0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs972278	0.86[AMR][1000 genomes];0.85[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	nsv830443	chr5:108326491-108496723	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv882692	chr5:108391660-108474166	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv882693	chr5:108391660-108502493	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882694	chr5:108391660-108524416	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv4953	chr5:108443905-108488747	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1027163	chr5:108445447-108839913	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 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	chr5:108435600-108446800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr5:108441600-108447400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr5:108441600-108455600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:108441800-108455600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:108442000-108446800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:108442000-108497400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:108442400-108449000	Weak transcription	Pancreas	Pancrea
8	chr5:108442800-108455600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:108444200-108447000	Weak transcription	HUVEC	blood vessel
10	chr5:108444200-108455600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:108445800-108448200	Weak transcription	Primary B cells from cord blood	blood

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