Variant report

Variant	rs7158947
Chromosome Location	chr14:84873072-84873073
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10131053	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10131334	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10144393	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12431750	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12432589	0.93[ASN][1000 genomes]
rs12879664	0.93[ASN][1000 genomes]
rs12880194	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12891714	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3000048	0.83[ASN][1000 genomes]
rs4243672	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4259973	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4328366	0.96[ASN][1000 genomes]
rs4350506	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4386065	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4410004	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4418993	0.85[AFR][1000 genomes]
rs4489939	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4500652	0.87[AFR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55682233	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs61984240	0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7148496	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7148700	0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7151303	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7160613	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs71908900	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8003576	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[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	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84865000-84876000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:84870400-84875600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr14:84870800-84876200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr14:84871400-84875800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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