Variant report

Variant	rs1914231
Chromosome Location	chr4:97370456-97370457
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs11943536	0.85[EUR][1000 genomes]
rs11943561	0.86[EUR][1000 genomes]
rs11943616	0.87[EUR][1000 genomes]
rs13102143	0.87[EUR][1000 genomes]
rs13127602	0.87[EUR][1000 genomes]
rs13136751	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1506302	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1516668	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17025342	0.88[EUR][1000 genomes]
rs17025392	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025422	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1911075	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1914230	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028711	0.88[EUR][1000 genomes]
rs2120492	0.87[EUR][1000 genomes]
rs2120493	0.84[EUR][1000 genomes]
rs2865738	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34167763	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34270338	0.82[EUR][1000 genomes]
rs34322283	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34929469	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35019362	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35666606	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4549388	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs66790817	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67248356	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68169129	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856653	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs71603290	0.86[EUR][1000 genomes]
rs7654559	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7667610	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7667933	0.86[EUR][1000 genomes]
rs938549	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][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	nsv1011487	chr4:97301762-97393803	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1009685	chr4:97308301-97392056	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97368800-97370600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:97370000-97371200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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