Variant report

Variant	rs7857345
Chromosome Location	chr9:22087473-22087474
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:22080093..22089919-chr9:22099951..22109614,29	MCF-7	breast:
2	chr9:22084984..22089844-chr9:22117518..22121243,5	MCF-7	breast:
3	chr9:22051930..22054348-chr9:22086021..22088331,2	MCF-7	breast:
4	chr9:22079850..22083849-chr9:22087242..22090618,5	MCF-7	breast:
5	chr9:21801904..21804122-chr9:22086706..22088895,2	MCF-7	breast:
6	chr9:22082310..22089949-chr9:22236353..22239754,11	MCF-7	breast:
7	chr9:21993116..21995180-chr9:22087072..22089483,2	MCF-7	breast:
8	chr9:22078947..22090885-chr9:22096375..22111093,52	MCF-7	breast:
9	chr9:22085206..22088406-chr9:22135474..22138114,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000264545	Chromatin interaction
ENSG00000099810	Chromatin interaction
ENSG00000147889	Chromatin interaction
ENSG00000240498	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1004638	0.95[ASN][1000 genomes]
rs10116277	1.00[YRI][hapmap]
rs10511701	0.85[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10738606	0.96[ASN][1000 genomes]
rs10738607	0.90[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10738608	0.91[ASN][1000 genomes]
rs10757272	0.90[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10757273	0.89[ASN][1000 genomes]
rs1333042	0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[ASN][1000 genomes]
rs1333043	0.86[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.98[ASN][1000 genomes]
rs1333047	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs1412832	0.86[CEU][hapmap]
rs1412834	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[ASN][1000 genomes]
rs1537371	0.98[ASN][1000 genomes]
rs1537373	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[ASN][1000 genomes]
rs1537374	0.95[ASN][1000 genomes]
rs1537375	0.95[ASN][1000 genomes]
rs1556516	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[ASN][1000 genomes]
rs2383207	0.94[ASN][1000 genomes]
rs4977575	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs4977757	0.80[ASN][1000 genomes]
rs6475606	1.00[YRI][hapmap]
rs6475609	0.98[ASN][1000 genomes]
rs7341786	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[ASN][1000 genomes]
rs7341791	0.98[ASN][1000 genomes]
rs7857118	0.94[ASN][1000 genomes]
rs7859362	0.91[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.98[ASN][1000 genomes]
rs7859727	0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv8426	chr9:21763810-22176200	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv531617	chr9:21985057-22809676	Genic enhancers Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22080600-22089400	Weak transcription	Dnd41	blood
2	chr9:22080600-22098600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:22085000-22087800	Weak transcription	Fetal Intestine Large	intestine
4	chr9:22085200-22088200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr9:22085400-22088000	Weak transcription	Stomach Mucosa	stomach
6	chr9:22085400-22088400	Weak transcription	HSMMtube	muscle
7	chr9:22085600-22088600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:22085800-22087600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:22085800-22088400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr9:22085800-22088400	Weak transcription	NHEK	skin
11	chr9:22085800-22089400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr9:22086000-22088200	Weak transcription	HMEC	breast
13	chr9:22086000-22088400	Weak transcription	Hela-S3	cervix
14	chr9:22086000-22097200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:22086200-22088200	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr9:22086400-22088000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:22086600-22089200	Enhancers	Fetal Intestine Small	intestine
18	chr9:22086800-22089800	Enhancers	Rectal Mucosa Donor 31	rectum

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