Variant report

Variant	rs7043679
Chromosome Location	chr9:117967041-117967042
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10739433	0.91[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10739434	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10759760	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10817722	0.89[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1271449	0.82[MEX][hapmap]
rs1335340	0.91[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1335344	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1335345	0.91[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1335346	0.85[YRI][hapmap]
rs1335351	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1335354	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1335355	0.86[CEU][hapmap];0.86[CHB][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1335356	0.95[CEU][hapmap];0.87[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1335360	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1360823	0.95[CEU][hapmap];0.87[CHB][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1414138	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1414148	1.00[CEU][hapmap];0.82[CHB][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1414150	0.95[CEU][hapmap];0.87[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1537731	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1537733	0.87[MEX][hapmap]
rs1591422	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1591423	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4978625	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4978626	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4979508	0.91[CEU][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4979511	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6478147	0.91[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6478150	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[CHD][hapmap];0.85[GIH][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6478151	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6478152	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6478153	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7027442	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7027882	0.91[CEU][hapmap];0.89[GIH][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7031000	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7043594	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][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]
rs7044001	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7044556	0.91[CEU][hapmap];0.86[GIH][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7045288	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7045508	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7045599	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7357796	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7470092	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs945258	0.91[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893769	chr9:117936903-117985886	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7043679	TNC	cis	lymphoblastoid	seeQTL
rs7043679	TXN	cis	cerebellum	SCAN

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117955600-117969000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:117959400-117968600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:117960600-117967400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:117960600-117969000	Weak transcription	Spleen	Spleen
5	chr9:117960800-117968800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr9:117960800-117969400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:117960800-117975800	Weak transcription	Fetal Kidney	kidney
8	chr9:117962200-117972600	Enhancers	NHDF-Ad	bronchial
9	chr9:117962400-117972400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:117963000-117972600	Enhancers	NHEK	skin
11	chr9:117963000-117972600	Enhancers	Osteobl	bone
12	chr9:117963000-117977200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr9:117963200-117969800	Enhancers	NHLF	lung
14	chr9:117963600-117969000	Weak transcription	Esophagus	oesophagus
15	chr9:117963800-117967800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr9:117964600-117970000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:117964600-117972800	Enhancers	NH-A	brain
18	chr9:117965200-117972400	Enhancers	HMEC	breast
19	chr9:117965800-117967200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr9:117966000-117967400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:117966000-117969000	Weak transcription	Placenta	Placenta
22	chr9:117966000-117969400	Weak transcription	Fetal Lung	lung
23	chr9:117966000-117970400	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:117966000-117973800	Weak transcription	Colon Smooth Muscle	Colon
25	chr9:117966200-117967400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr9:117966200-117973600	Weak transcription	Fetal Stomach	stomach
27	chr9:117966400-117972800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr9:117966800-117968200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:117966800-117968200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr9:117966800-117969800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:117967000-117968200	Enhancers	HSMM	muscle
32	chr9:117967000-117968400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:117967000-117968400	Enhancers	Placenta Amnion	Placenta Amnion
34	chr9:117967000-117968800	Enhancers	GM12878-XiMat	blood
35	chr9:117967000-117972600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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