Variant report

Variant	rs72845315
Chromosome Location	chr17:63244975-63244976
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs11079561	0.86[ASN][1000 genomes]
rs16961703	0.86[ASN][1000 genomes]
rs16961727	0.86[ASN][1000 genomes]
rs16961732	0.86[ASN][1000 genomes]
rs16961878	0.86[ASN][1000 genomes]
rs16961897	0.86[ASN][1000 genomes]
rs17689671	0.86[ASN][1000 genomes]
rs28476544	0.86[ASN][1000 genomes]
rs28895913	0.86[ASN][1000 genomes]
rs55853855	0.86[ASN][1000 genomes]
rs55864812	0.86[ASN][1000 genomes]
rs56202104	0.86[ASN][1000 genomes]
rs56205487	0.86[ASN][1000 genomes]
rs56408543	0.86[ASN][1000 genomes]
rs56684368	0.86[ASN][1000 genomes]
rs57333496	0.86[ASN][1000 genomes]
rs58012124	0.86[ASN][1000 genomes]
rs60495439	0.86[ASN][1000 genomes]
rs60919543	0.86[ASN][1000 genomes]
rs62063085	0.86[ASN][1000 genomes]
rs62063086	0.86[ASN][1000 genomes]
rs62065142	0.86[ASN][1000 genomes]
rs62065143	0.86[ASN][1000 genomes]
rs62065144	0.86[ASN][1000 genomes]
rs62065147	0.86[ASN][1000 genomes]
rs67111745	0.86[ASN][1000 genomes]
rs7207480	0.86[ASN][1000 genomes]
rs7207744	0.86[ASN][1000 genomes]
rs7211786	0.86[ASN][1000 genomes]
rs7212442	0.86[ASN][1000 genomes]
rs7213152	0.86[ASN][1000 genomes]
rs7215623	0.86[ASN][1000 genomes]
rs7219197	0.86[ASN][1000 genomes]
rs7219498	0.86[ASN][1000 genomes]
rs7219691	0.86[ASN][1000 genomes]
rs7220948	0.86[ASN][1000 genomes]
rs7221051	0.86[ASN][1000 genomes]
rs7221258	0.86[ASN][1000 genomes]
rs7221276	0.86[ASN][1000 genomes]
rs7221428	0.86[ASN][1000 genomes]
rs7221810	0.86[ASN][1000 genomes]
rs72854623	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7342966	0.86[ASN][1000 genomes]
rs8065208	0.86[ASN][1000 genomes]
rs8071511	0.86[ASN][1000 genomes]
rs8072237	0.86[ASN][1000 genomes]
rs8074052	0.86[ASN][1000 genomes]
rs8077032	0.86[ASN][1000 genomes]
rs8078209	0.86[ASN][1000 genomes]
rs8078535	0.86[ASN][1000 genomes]
rs8078847	0.86[ASN][1000 genomes]
rs8081224	0.86[ASN][1000 genomes]
rs8082275	0.86[ASN][1000 genomes]
rs8082401	0.86[ASN][1000 genomes]
rs9897086	0.86[ASN][1000 genomes]
rs9897299	0.86[ASN][1000 genomes]
rs9898094	0.86[ASN][1000 genomes]
rs9905007	0.86[ASN][1000 genomes]
rs9905226	0.86[ASN][1000 genomes]
rs9914176	0.86[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	nsv530764	chr17:62939944-63278472	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv482610	chr17:63214370-63372334	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63240600-63245200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:63240800-63245200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr17:63241200-63245000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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