Variant report

Variant	rs55658944
Chromosome Location	chr9:104097740-104097741
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10521055	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11787626	1.00[ASN][1000 genomes]
rs11788485	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11792021	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11792023	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11793965	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11794505	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16920200	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1935241	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1935242	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2900307	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4403470	1.00[ASN][1000 genomes]
rs4416881	1.00[ASN][1000 genomes]
rs4451365	1.00[ASN][1000 genomes]
rs4474082	1.00[ASN][1000 genomes]
rs4612403	1.00[ASN][1000 genomes]
rs55786195	0.85[AFR][1000 genomes]
rs55947778	0.85[AFR][1000 genomes]
rs55952033	0.82[AFR][1000 genomes]
rs56135593	0.88[EUR][1000 genomes]
rs58013833	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58772170	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73492631	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73492632	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73492646	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73509627	1.00[ASN][1000 genomes]
rs73509628	1.00[ASN][1000 genomes]
rs73509629	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037157	chr9:104045761-104149233	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr9:104095600-104101800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:104097400-104098600	Enhancers	HepG2	liver

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