Variant report

Variant	rs9293938
Chromosome Location	chr6:74424355-74424356
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:74405796..74408652-chr6:74422583..74424647,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000156535	Chromatin interaction
ENSG00000231652	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10455283	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13201723	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6923034	0.94[JPT][hapmap];0.82[TSI][hapmap];0.83[ASN][1000 genomes]
rs7767106	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9293937	0.93[CHB][hapmap];0.86[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9442953	0.94[JPT][hapmap]
rs9446995	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9446996	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9447001	1.00[JPT][hapmap];0.82[YRI][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886158	chr6:74126084-74436825	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
2	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
3	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
5	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers 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 target site	172 gene(s)	inside rSNPs	diseases
6	nsv1029927	chr6:74300496-74424355	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv463154	chr6:74412048-74775904	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv603695	chr6:74412048-74775904	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74407200-74424800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr6:74408000-74446800	Weak transcription	Dnd41	blood
3	chr6:74414800-74474600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:74415200-74432200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:74420400-74425200	Enhancers	Primary hematopoietic stem cells	blood
6	chr6:74421000-74424600	Weak transcription	Hela-S3	cervix
7	chr6:74421000-74432200	Weak transcription	HSMM	muscle
8	chr6:74422200-74424400	Enhancers	Adipose Nuclei	Adipose
9	chr6:74422200-74424600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:74422200-74425000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:74422400-74424400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr6:74422400-74424400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:74422600-74425400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:74422600-74432000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:74423000-74424400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:74423000-74424400	Enhancers	Brain Substantia Nigra	brain
17	chr6:74423000-74424800	Genic enhancers	NHDF-Ad	bronchial
18	chr6:74423000-74425000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:74423000-74425200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:74423200-74424400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr6:74423200-74424400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr6:74423200-74424400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr6:74423200-74424400	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr6:74423200-74424400	Enhancers	Lung	lung
25	chr6:74423200-74424400	Flanking Active TSS	HUVEC	blood vessel
26	chr6:74423200-74424800	Enhancers	NH-A	brain
27	chr6:74423200-74425200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:74423200-74425400	Enhancers	Osteobl	bone
29	chr6:74423400-74424400	Enhancers	Primary B cells from peripheral blood	blood
30	chr6:74423400-74424400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:74423400-74424600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:74423400-74424600	Enhancers	Placenta Amnion	Placenta Amnion
33	chr6:74423400-74424800	Flanking Active TSS	A549	lung
34	chr6:74423600-74424400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:74423600-74424400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr6:74423600-74424400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr6:74423600-74424400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:74423600-74424600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr6:74423600-74441000	Weak transcription	Stomach Smooth Muscle	stomach
40	chr6:74423800-74424400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:74423800-74424400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:74423800-74424400	Enhancers	Thymus	Thymus
43	chr6:74423800-74424600	Genic enhancers	HMEC	breast
44	chr6:74423800-74424800	Enhancers	NHLF	lung
45	chr6:74424000-74424400	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr6:74424000-74424400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:74424000-74424600	Enhancers	Fetal Heart	heart
48	chr6:74424000-74425400	Enhancers	NHEK	skin
49	chr6:74424200-74424400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr6:74424200-74424600	Weak transcription	Esophagus	oesophagus

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