Variant report

Variant	rs10904721
Chromosome Location	chr10:16403744-16403745
allele	A/T
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:32)

rs_ID	r²[population]
rs11253933	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11253938	0.80[ASN][1000 genomes]
rs11253941	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11253942	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11253944	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11253946	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11253950	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11253951	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11253952	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11253953	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11253954	0.81[ASN][1000 genomes]
rs11253955	0.81[ASN][1000 genomes]
rs11253956	0.80[ASN][1000 genomes]
rs11253957	0.80[ASN][1000 genomes]
rs11253958	0.80[ASN][1000 genomes]
rs12218570	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12219022	0.80[ASN][1000 genomes]
rs12242634	0.92[EUR][1000 genomes]
rs12570048	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12783760	0.81[ASN][1000 genomes]
rs17138484	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17138492	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17138511	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6602101	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7082220	0.82[ASN][1000 genomes]
rs7099690	0.82[ASN][1000 genomes]
rs72768690	0.81[EUR][1000 genomes]
rs72768692	0.81[EUR][1000 genomes]
rs72770421	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72770445	0.80[EUR][1000 genomes]
rs7909328	0.95[EUR][1000 genomes]
rs988459	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530146	chr10:15722937-16522747	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv870420	chr10:16225427-16541252	Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv894904	chr10:16233175-16477106	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	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	chr10:16403400-16408800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:16403400-16428600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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