Variant report

Variant	rs10434137
Chromosome Location	chr4:152148622-152148623
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:152147209-152150071	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr4:152148535-152149562	HUVEC	blood vessel:	n/a	n/a

Variant related genes	Relation type
SH3D19	TF binding region

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10016092	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10020297	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10020317	0.85[ASW][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap]
rs10461254	0.80[AFR][1000 genomes]
rs10461255	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs10520101	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10520102	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10776522	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10857253	0.89[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs11099792	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11099793	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11099796	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11733964	0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs11734577	0.85[ASW][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap]
rs11934792	0.93[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs11945206	0.99[ASN][1000 genomes]
rs12505974	0.85[ASW][hapmap];0.94[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs12508270	0.85[JPT][hapmap]
rs12644496	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12647306	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.80[AFR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13101417	0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs13103344	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13111753	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13122609	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13125574	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13141515	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs13145829	0.94[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap]
rs17633530	0.85[JPT][hapmap]
rs17633600	0.85[JPT][hapmap]
rs2280280	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs2280283	0.85[JPT][hapmap]
rs2407222	0.99[ASN][1000 genomes]
rs2407223	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2407407	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407408	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407409	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407410	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407412	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407413	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2407417	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407418	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2407431	0.83[EUR][1000 genomes]
rs2897655	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2897656	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2897659	0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs3736502	0.85[JPT][hapmap]
rs3792611	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4266274	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4312738	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4467540	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4591577	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4696234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4696239	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4696658	0.85[ASW][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs6535764	0.85[JPT][hapmap]
rs6846323	0.85[ASW][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap]
rs6847934	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7439970	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7656771	0.85[JPT][hapmap]
rs7664483	0.85[ASW][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs7669180	0.85[ASW][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap]
rs7688786	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7691584	0.95[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS 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	38 gene(s)	inside rSNPs	diseases
4	nsv948719	chr4:151693149-152161625	Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	nsv881526	chr4:151968295-152489087	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv1016220	chr4:151997139-152164126	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv537306	chr4:151997139-152164126	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
9	nsv870229	chr4:152114410-152161072	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152117600-152148800	Weak transcription	Esophagus	oesophagus
2	chr4:152120800-152153800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:152129000-152148800	Weak transcription	Fetal Intestine Large	intestine
4	chr4:152129000-152168000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr4:152129200-152148800	Weak transcription	Liver	Liver
6	chr4:152129400-152167800	Weak transcription	Right Ventricle	heart
7	chr4:152130200-152187800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr4:152136600-152158000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:152137400-152148800	Weak transcription	Left Ventricle	heart
10	chr4:152141000-152167400	Weak transcription	HepG2	liver
11	chr4:152144800-152149200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr4:152144800-152163400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:152145800-152148800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:152145800-152148800	Active TSS	NHDF-Ad	bronchial
15	chr4:152145800-152149600	Active TSS	Right Atrium	heart
16	chr4:152146000-152148800	Active TSS	Adipose Nuclei	Adipose
17	chr4:152146000-152149000	Active TSS	Ovary	ovary
18	chr4:152146000-152149200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:152146000-152149200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:152146000-152149400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:152146200-152149800	Flanking Active TSS	HUVEC	blood vessel
22	chr4:152146600-152149600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:152146800-152149000	Active TSS	Fetal Muscle Leg	muscle
24	chr4:152146800-152149200	Active TSS	Brain Angular Gyrus	brain
25	chr4:152147000-152148800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:152147000-152149000	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
27	chr4:152147000-152149000	Active TSS	Placenta Amnion	Placenta Amnion
28	chr4:152147000-152149200	Active TSS	Brain Cingulate Gyrus	brain
29	chr4:152147000-152149200	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr4:152147000-152149400	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr4:152147200-152149000	Active TSS	Brain Substantia Nigra	brain
32	chr4:152147200-152149000	Active TSS	Psoas Muscle	Psoas
33	chr4:152147200-152149200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr4:152147200-152149400	Active TSS	Brain Hippocampus Middle	brain
35	chr4:152147200-152150200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr4:152147200-152150200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:152147200-152160200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr4:152147400-152149600	Active TSS	Aorta	Aorta
39	chr4:152147400-152149600	Enhancers	Colon Smooth Muscle	Colon
40	chr4:152147400-152150200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr4:152147600-152149200	Active TSS	Brain Anterior Caudate	brain
42	chr4:152147600-152149800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:152147600-152150200	Enhancers	Fetal Heart	heart
44	chr4:152147600-152150800	Enhancers	Fetal Stomach	stomach
45	chr4:152147800-152149000	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr4:152148000-152148800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr4:152148000-152148800	Weak transcription	Fetal Muscle Trunk	muscle
48	chr4:152148000-152148800	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr4:152148000-152148800	Enhancers	NHEK	skin
50	chr4:152148000-152149000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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