Variant report

Variant	rs7837973
Chromosome Location	chr8:63648985-63648986
allele	A/T
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]
rs10093544	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10107976	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10957238	0.81[ASN][1000 genomes]
rs11780909	0.93[ASN][1000 genomes]
rs11985179	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12386973	0.93[ASN][1000 genomes]
rs12708012	0.81[ASN][1000 genomes]
rs1351352	0.82[ASN][1000 genomes]
rs1480118	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1480124	0.81[ASN][1000 genomes]
rs1480125	0.85[ASN][1000 genomes]
rs1480127	0.85[ASN][1000 genomes]
rs1480196	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1531651	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1600537	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1600539	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1600540	0.81[ASN][1000 genomes]
rs1904572	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1904574	0.93[ASN][1000 genomes]
rs2054523	0.93[ASN][1000 genomes]
rs2127560	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2352401	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4621803	0.85[ASN][1000 genomes]
rs6472047	0.93[ASN][1000 genomes]
rs6996317	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6996526	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7001779	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7003752	0.94[ASN][1000 genomes]
rs7005463	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7008248	0.93[ASN][1000 genomes]
rs7008492	0.93[ASN][1000 genomes]
rs7009434	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7012264	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7821374	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7828204	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9298066	0.81[EUR][1000 genomes]
rs931131	0.93[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	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831340	chr8:63515126-63702660	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63646400-63649000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr8:63646600-63649000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr8:63646600-63649200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:63648200-63649200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:63648400-63649000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr8:63648400-63649200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:63648400-63649200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:63648600-63649600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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