Variant report

Variant	rs4981956
Chromosome Location	chr14:32744210-32744211
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1007279	0.86[CEU][hapmap];0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2208869	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2383310	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4981953	0.86[CEU][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6571502	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6571507	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7144586	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs7155347	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7160483	0.86[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7161546	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8005191	0.93[EUR][1000 genomes]
rs8012126	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8014494	0.81[EUR][1000 genomes]
rs8023125	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[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	esv3527777	chr14:32669175-32761850	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3527778	chr14:32669175-32761850	Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32742800-32752800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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