Variant report

Variant	rs10735885
Chromosome Location	chr12:40151546-40151547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:40150704..40153291-chr12:40154955..40157099,2	K562	blood:

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10219652	1.00[CEU][hapmap];0.88[JPT][hapmap];0.87[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10444570	0.94[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10747825	0.88[JPT][hapmap]
rs10747877	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10747878	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10783959	1.00[CEU][hapmap];0.81[YRI][hapmap]
rs10783969	0.81[JPT][hapmap]
rs10783994	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10784001	0.88[JPT][hapmap]
rs10784016	0.88[JPT][hapmap]
rs10784019	0.88[JPT][hapmap]
rs10784034	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10784051	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10784059	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10877383	1.00[CEU][hapmap];0.88[JPT][hapmap];0.96[YRI][hapmap]
rs10877410	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11173013	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs11173259	0.87[EUR][1000 genomes]
rs11173376	0.82[EUR][1000 genomes]
rs11173394	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173401	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11173411	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11173423	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173424	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11173428	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173433	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11173434	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173440	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173446	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173459	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11173494	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11173507	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11173541	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11173550	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11173551	0.91[ASN][1000 genomes]
rs11173553	0.89[ASN][1000 genomes]
rs11532458	0.93[ASN][1000 genomes]
rs12229203	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12229301	0.88[JPT][hapmap]
rs12229418	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12230687	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12299938	0.85[ASN][1000 genomes]
rs12823801	1.00[CEU][hapmap];0.88[JPT][hapmap];0.87[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4077987	0.88[JPT][hapmap]
rs4238072	0.94[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4238073	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4254134	0.83[CEU][hapmap]
rs4255599	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4255600	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4312128	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4322460	0.89[ASN][1000 genomes]
rs4322461	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4337105	0.88[JPT][hapmap]
rs4357762	0.88[JPT][hapmap]
rs4381428	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4388963	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4391875	0.82[ASN][1000 genomes]
rs4397916	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4405390	0.94[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4405391	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4411336	1.00[CEU][hapmap];0.88[JPT][hapmap];0.96[YRI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4417381	0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4417382	0.87[JPT][hapmap]
rs4495951	0.88[JPT][hapmap]
rs4556618	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4594067	0.88[JPT][hapmap]
rs4767949	0.94[CEU][hapmap];0.82[JPT][hapmap];0.89[YRI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4768168	0.88[JPT][hapmap]
rs4768169	0.88[JPT][hapmap]
rs4768170	0.80[ASN][1000 genomes]
rs57244766	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58418587	0.80[ASN][1000 genomes]
rs61931185	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61931208	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61931211	0.82[ASN][1000 genomes]
rs61933154	0.80[ASN][1000 genomes]
rs61933157	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61933158	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6421196	0.88[JPT][hapmap]
rs6581250	1.00[CEU][hapmap];0.88[JPT][hapmap];0.87[YRI][hapmap]
rs6581263	0.81[JPT][hapmap]
rs6581271	0.88[JPT][hapmap]
rs6581294	0.80[ASN][1000 genomes]
rs6581357	0.83[CEU][hapmap]
rs7298453	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7301886	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7302849	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7308955	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7485345	0.87[JPT][hapmap]
rs7486631	0.81[JPT][hapmap]
rs7487812	1.00[CEU][hapmap];0.87[YRI][hapmap]
rs7487999	0.88[JPT][hapmap]
rs7952735	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7961346	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs7964129	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7969282	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7980636	0.88[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531527	chr12:39680812-40182822	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1037457	chr12:39898349-40245401	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv541480	chr12:39898349-40245401	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv899024	chr12:40046408-40188870	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1053603	chr12:40082673-40197609	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv427907	chr12:40122713-40199621	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv428280	chr12:40122713-40199621	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40130800-40156400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr12:40137200-40154200	Weak transcription	Liver	Liver
3	chr12:40143800-40156800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr12:40144200-40156200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:40144200-40157600	Weak transcription	Pancreas	Pancrea
6	chr12:40144800-40166400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:40145000-40175000	Weak transcription	Right Ventricle	heart
8	chr12:40145200-40154000	Weak transcription	Fetal Intestine Large	intestine
9	chr12:40145600-40157400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr12:40146000-40166800	Weak transcription	Ovary	ovary
11	chr12:40146200-40157200	Weak transcription	Aorta	Aorta
12	chr12:40146200-40157200	Weak transcription	Left Ventricle	heart
13	chr12:40146200-40159000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:40147400-40157200	Weak transcription	Adipose Nuclei	Adipose
15	chr12:40147800-40153400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr12:40148000-40157000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:40148200-40157000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr12:40150000-40157200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:40150200-40160400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:40151400-40160600	Weak transcription	NHDF-Ad	bronchial

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