Variant report

Variant	rs7156910
Chromosome Location	chr14:72751678-72751679
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:72749616..72751897-chr14:72756117..72758691,2	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10146126	0.82[EUR][1000 genomes]
rs1029616	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs1029617	0.83[AFR][1000 genomes]
rs12184980	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs1879290	0.84[AFR][1000 genomes]
rs1879291	0.82[AFR][1000 genomes]
rs1879292	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs2079499	0.83[YRI][hapmap]
rs2238204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2238205	0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2238206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2238207	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4578585	0.88[AFR][1000 genomes]
rs4899430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6574060	0.89[AFR][1000 genomes]
rs6574061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6574065	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7144038	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs7149034	0.84[YRI][hapmap]
rs7151952	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7152907	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs7156275	0.88[AFR][1000 genomes]
rs737499	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs847348	0.82[EUR][1000 genomes]
rs847349	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs847350	0.83[EUR][1000 genomes]
rs847360	0.88[CHB][hapmap];0.89[JPT][hapmap]
rs847362	0.88[CHB][hapmap];0.89[JPT][hapmap]
rs847364	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs917284	0.80[YRI][hapmap]

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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1041492	chr14:72634606-72768970	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72747600-72752600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72749400-72752800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr14:72750800-72751800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
4	chr14:72751000-72752800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:72751600-72752200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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