Variant report

Variant	rs3007670
Chromosome Location	chr1:151897616-151897617
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:151897183..151899597-chr1:151964154..151966740,2	MCF-7	breast:
2	chr1:151896485..151898920-chr1:151899927..151901440,2	MCF-7	breast:
3	chr1:151896761..151899276-chr1:152001474..152003211,2	MCF-7	breast:
4	chr1:151879281..151886788-chr1:151893548..151899266,9	MCF-7	breast:
5	chr1:151896603..151899369-chr1:152019666..152021971,2	MCF-7	breast:
6	chr1:151896649..151898328-chr1:151903426..151905406,2	K562	blood:

Variant related genes	Relation type
ENSG00000163191	Chromatin interaction
ENSG00000197747	Chromatin interaction
ENSG00000159445	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1038747	0.83[CHB][hapmap];0.88[JPT][hapmap]
rs10494270	0.90[CHB][hapmap]
rs1060870	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10788817	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10788818	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10788820	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10888445	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs11204914	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11204915	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11204922	0.85[JPT][hapmap]
rs11589720	0.81[ASN][1000 genomes]
rs12067594	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12116923	0.82[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12562586	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13320	0.83[CHB][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1387833	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1490189	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16833668	0.86[CHB][hapmap]
rs16833728	0.81[CHB][hapmap]
rs1907040	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2130525	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2279501	0.86[CHB][hapmap];0.90[JPT][hapmap];0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2279502	0.91[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2338019	0.85[JPT][hapmap]
rs2338201	0.91[AMR][1000 genomes]
rs2338209	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2932565	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2932570	0.80[JPT][hapmap]
rs2932576	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2932577	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2932579	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2932583	0.82[ASN][1000 genomes]
rs2932586	0.82[ASN][1000 genomes]
rs2932590	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs2999506	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2999526	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs2999528	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs2999531	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs2999541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2999542	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2999544	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2999545	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2999546	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3007685	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3007691	0.82[ASN][1000 genomes]
rs3007708	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs3007711	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845409	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845713	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6663064	0.86[CHB][hapmap]
rs6685187	0.83[CHB][hapmap];0.89[JPT][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6686874	0.86[CHB][hapmap]
rs6698740	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7523082	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7541099	0.81[CHB][hapmap]
rs7541453	0.82[AMR][1000 genomes]
rs7542137	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs902313	0.81[CHB][hapmap]
rs9435963	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9435964	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9943221	0.91[CHB][hapmap]
rs9943281	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[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	nsv1007097	chr1:151832796-152227977	Strong transcription Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
2	nsv1012327	chr1:151835544-152200890	Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
3	nsv535159	chr1:151835544-152200890	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
4	nsv547852	chr1:151843044-151955230	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
5	nsv872441	chr1:151850072-152034430	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	191 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs3007670	THEM4	cis	Esophagus Muscularis	GTEx
rs3007670	THEM4	cis	Nerve Tibial	GTEx
rs3007670	THEM4	cis	uninvolved skin	skin_eQTL
rs3007670	THEM4	cis	multi-tissue	Pritchard
rs3007670	THEM4	Cis_1M	lymphoblastoid	RTeQTL
rs3007670	S100A10	Cis_1M	lymphoblastoid	RTeQTL
rs3007670	S100A10	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151895800-151898000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:151896000-151899000	Weak transcription	K562	blood
3	chr1:151897000-151898200	Enhancers	NHEK	skin
4	chr1:151897200-151898200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:151897200-151898200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:151897200-151898200	Flanking Active TSS	GM12878-XiMat	blood
7	chr1:151897200-151898200	Enhancers	HMEC	breast
8	chr1:151897400-151898200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:151897400-151898200	Enhancers	Primary B cells from peripheral blood	blood
10	chr1:151897400-151898200	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr1:151897400-151898200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:151897400-151898400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr1:151897400-151898400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr1:151897400-151898400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr1:151897400-151898400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr1:151897400-151898400	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr1:151897600-151897800	Enhancers	Primary B cells from cord blood	blood
18	chr1:151897600-151898000	Enhancers	Primary T cells fromperipheralblood	blood
19	chr1:151897600-151898200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr1:151897600-151898400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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