Variant report

Variant	rs4943918
Chromosome Location	chr11:85171821-85171822
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:85169801..85172207-chr11:85373723..85376174,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000137504	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10501595	0.94[CHB][hapmap]
rs11234359	1.00[CHB][hapmap];0.81[CHD][hapmap]
rs1213236	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1354397	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs1647941	0.95[ASN][1000 genomes]
rs166977	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17208492	0.94[CHB][hapmap]
rs17208519	0.94[CHB][hapmap]
rs17810659	0.94[CHB][hapmap];0.83[YRI][hapmap]
rs1793210	0.82[ASN][1000 genomes]
rs1806414	0.81[AFR][1000 genomes]
rs1892872	0.94[CHB][hapmap]
rs190813	0.86[ASN][1000 genomes]
rs1991923	0.94[CHB][hapmap]
rs2113920	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2290823	0.94[CHB][hapmap]
rs2433016	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs286044	0.83[ASN][1000 genomes]
rs286497	0.87[ASN][1000 genomes]
rs286499	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs286513	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs286515	1.00[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs286516	0.91[ASN][1000 genomes]
rs286541	0.83[AFR][1000 genomes]
rs4943925	0.92[CHB][hapmap]
rs4944516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944529	0.94[CHB][hapmap];0.91[YRI][hapmap]
rs4944531	0.94[CHB][hapmap]
rs496814	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs516620	0.84[JPT][hapmap]
rs531331	0.84[CHB][hapmap];0.83[CHD][hapmap];0.84[JPT][hapmap]
rs550981	0.94[CHB][hapmap]
rs7104879	1.00[ASN][1000 genomes]
rs7110363	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7116340	0.94[ASN][1000 genomes]
rs7122822	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7130198	0.95[ASN][1000 genomes]
rs7943586	0.94[CHB][hapmap]
rs7948778	0.94[CHB][hapmap]
rs881121	0.84[ASW][hapmap];0.94[CHB][hapmap]
rs947861	0.94[CHB][hapmap]
rs947863	0.94[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv1035905	chr11:85130543-85220773	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1050363	chr11:85163437-85293233	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv541111	chr11:85163437-85293233	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85163600-85173800	Weak transcription	Left Ventricle	heart
2	chr11:85171400-85182800	Weak transcription	Ovary	ovary

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