Variant report

Variant	rs10992090
Chromosome Location	chr9:94536329-94536330
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94536230..94537049-chr9:94645022..94645936,2	MCF-7	breast:
2	chr9:94534777..94536619-chr9:94540454..94542317,2	MCF-7	breast:
3	chr9:94533140..94534672-chr9:94535673..94537845,2	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10512217	0.91[YRI][hapmap];0.83[AFR][1000 genomes]
rs10820902	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10820903	0.81[AMR][1000 genomes]
rs10992086	0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs10992095	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10992104	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10992108	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10992109	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12235606	0.83[AFR][1000 genomes]
rs12235611	0.83[AFR][1000 genomes]
rs12237459	0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs12237573	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12238428	0.82[YRI][hapmap]
rs12685213	1.00[ASW][hapmap];1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs12685849	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs16907741	0.83[AFR][1000 genomes]
rs16907768	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16907776	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[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2178196	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2312730	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs3802377	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[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3802378	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[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3935544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4322069	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4398991	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4400454	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4452868	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.85[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4595186	0.83[YRI][hapmap];0.82[AFR][1000 genomes]
rs4601388	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs57810120	0.97[EUR][1000 genomes]
rs58210546	0.87[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs58462029	0.97[EUR][1000 genomes]
rs60092492	0.97[EUR][1000 genomes]
rs60617711	0.97[EUR][1000 genomes]
rs73511086	0.87[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs73513203	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73513246	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73651508	0.87[AFR][1000 genomes];0.97[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	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv531631	chr9:94373847-94633213	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1036176	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv540171	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94527600-94538800	Weak transcription	K562	blood
2	chr9:94529400-94539800	Enhancers	Colon Smooth Muscle	Colon
3	chr9:94532200-94537000	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr9:94532200-94539200	Enhancers	Fetal Heart	heart
5	chr9:94532800-94536400	Enhancers	Fetal Lung	lung
6	chr9:94533000-94542800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:94533000-94543600	Weak transcription	Right Atrium	heart
8	chr9:94533400-94537600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:94533400-94537600	Enhancers	Rectal Smooth Muscle	rectum
10	chr9:94533400-94549600	Weak transcription	Colonic Mucosa	Colon
11	chr9:94533600-94545400	Enhancers	Stomach Smooth Muscle	stomach
12	chr9:94534000-94536600	Enhancers	Placenta	Placenta
13	chr9:94534200-94537400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr9:94534200-94538200	Genic enhancers	Fetal Stomach	stomach
15	chr9:94534400-94546800	Weak transcription	Fetal Kidney	kidney
16	chr9:94534600-94537600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:94534600-94538000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:94534600-94538800	Weak transcription	Spleen	Spleen
19	chr9:94534600-94539400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:94534800-94537400	Weak transcription	Gastric	stomach
21	chr9:94534800-94537600	Weak transcription	Ovary	ovary
22	chr9:94535000-94536400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:94535000-94538000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr9:94535000-94538600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:94535000-94539400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:94535200-94536600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:94535400-94536400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:94535600-94537600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:94536000-94536400	Bivalent Enhancer	HSMMtube	muscle
30	chr9:94536000-94537800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:94536000-94543200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr9:94536000-94543600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr9:94536200-94537400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:94536200-94537600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr9:94536200-94537600	Weak transcription	Esophagus	oesophagus
36	chr9:94536200-94537600	Weak transcription	Fetal Intestine Large	intestine
37	chr9:94536200-94537800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr9:94536200-94537800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:94536200-94537800	Strong transcription	Fetal Intestine Small	intestine
40	chr9:94536200-94544600	Weak transcription	Placenta Amnion	Placenta Amnion

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