Variant report

Variant	rs73878307
Chromosome Location	chr3:161076899-161076900
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:161041894..161044446-chr3:161076689..161079941,3	MCF-7	breast:
2	chr3:160817108..160819298-chr3:161076893..161078523,2	MCF-7	breast:
3	chr3:64035675..64038032-chr3:161075125..161077341,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000240138	Chromatin interaction
ENSG00000169255	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs12632351	0.81[AFR][1000 genomes]
rs12632537	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12632686	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12634006	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16832203	0.88[EUR][1000 genomes]
rs28713364	0.82[EUR][1000 genomes]
rs56230831	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs57278490	0.95[EUR][1000 genomes]
rs57496534	0.95[EUR][1000 genomes]
rs57803909	0.95[EUR][1000 genomes]
rs57916312	0.86[EUR][1000 genomes]
rs57974280	0.82[EUR][1000 genomes]
rs58350275	0.95[EUR][1000 genomes]
rs58550445	0.93[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs58557417	0.88[EUR][1000 genomes]
rs58562874	0.95[EUR][1000 genomes]
rs58878734	0.82[EUR][1000 genomes]
rs59541314	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59761692	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59964190	0.95[EUR][1000 genomes]
rs60400555	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60612225	0.95[EUR][1000 genomes]
rs60684226	0.95[EUR][1000 genomes]
rs61048679	1.00[AMR][1000 genomes]
rs61217744	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788738	0.82[EUR][1000 genomes]
rs72494864	0.81[ASN][1000 genomes]
rs73023224	0.82[EUR][1000 genomes]
rs73878306	0.86[ASN][1000 genomes]
rs73878308	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73878311	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73878313	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73878321	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73878322	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73878324	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73878325	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73878328	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7625217	0.95[EUR][1000 genomes]
rs873183	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs896080	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9834806	0.82[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	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv963570	chr3:161076656-161088849	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161059800-161089200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:161064400-161083000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:161068200-161083200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:161068400-161083200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr3:161068800-161079000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr3:161071600-161077000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr3:161076000-161077400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:161076200-161077200	Weak transcription	Esophagus	oesophagus
9	chr3:161076200-161083200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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