Variant report

Variant	rs1431536
Chromosome Location	chr7:14463949-14463950
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10228053	0.86[CEU][hapmap]
rs10243451	0.84[CEU][hapmap]
rs11761424	0.80[AMR][1000 genomes]
rs12111648	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12532234	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12532527	0.82[CEU][hapmap]
rs12535183	0.82[CEU][hapmap]
rs12535778	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12536559	0.81[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12536670	0.95[CEU][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12540165	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13232324	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13233368	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1367776	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1367777	0.81[CEU][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1367778	0.95[CEU][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1431534	0.95[CEU][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1431535	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1560575	0.84[CEU][hapmap]
rs196756	0.80[CEU][hapmap];0.85[EUR][1000 genomes]
rs2043221	1.00[YRI][hapmap];0.84[AMR][1000 genomes]
rs2067698	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2116531	0.80[AMR][1000 genomes]
rs34628921	0.81[CEU][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34886902	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35182111	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35469417	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35690340	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs36198503	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56352403	0.80[AMR][1000 genomes]
rs58641244	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6962080	0.88[EUR][1000 genomes]
rs73068025	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73068026	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73068027	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7780569	0.82[CEU][hapmap]
rs891808	0.84[CEU][hapmap]

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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 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	chr7:14459600-14465000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:14459600-14465200	Weak transcription	Fetal Heart	heart

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