Variant report

Variant	rs7156008
Chromosome Location	chr14:63509861-63509862
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:63507970..63510136-chr14:63516834..63518803,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1007062	0.84[CEU][hapmap]
rs10130015	0.85[CEU][hapmap]
rs10141458	0.92[CEU][hapmap]
rs10873166	0.84[JPT][hapmap]
rs11158468	0.84[CEU][hapmap]
rs11158469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12587142	0.92[CEU][hapmap]
rs12587171	0.92[CEU][hapmap]
rs1950986	0.85[CEU][hapmap]
rs1950987	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[JPT][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1956673	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1956674	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1956675	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3850312	0.89[JPT][hapmap]
rs3906693	0.84[CEU][hapmap]
rs3910327	1.00[CEU][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3915801	0.89[JPT][hapmap]
rs4127778	0.84[JPT][hapmap]
rs4127780	0.89[JPT][hapmap]
rs4609762	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5010675	0.82[CEU][hapmap]
rs6573475	0.84[CEU][hapmap]
rs6573476	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[JPT][hapmap];0.88[YRI][hapmap]
rs6573477	0.91[CEU][hapmap]
rs7154634	1.00[CEU][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs717059	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8004263	0.92[CEU][hapmap];0.82[AMR][1000 genomes]
rs8005258	0.92[CEU][hapmap]
rs8015817	0.85[JPT][hapmap]
rs8018212	0.84[CEU][hapmap]
rs8020935	0.85[JPT][hapmap]
rs8021399	0.92[CEU][hapmap];0.82[AMR][1000 genomes]
rs8021914	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 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	chr14:63503000-63511000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:63507000-63510800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr14:63509800-63510000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:63509800-63510600	Weak transcription	Hela-S3	cervix
5	chr14:63509800-63511200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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