Variant report

Variant	rs62577465
Chromosome Location	chr9:104502337-104502338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10512288	0.93[EUR][1000 genomes]
rs16920674	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2069324	0.85[EUR][1000 genomes]
rs2069325	0.85[EUR][1000 genomes]
rs55734521	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55971755	0.82[AFR][1000 genomes]
rs56236943	0.93[EUR][1000 genomes]
rs59275233	0.83[EUR][1000 genomes]
rs62576354	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62576359	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62577460	0.85[EUR][1000 genomes]
rs62577463	0.91[EUR][1000 genomes]
rs62577464	0.89[EUR][1000 genomes]
rs62582206	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62582209	0.85[EUR][1000 genomes]
rs6479062	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6479064	0.85[EUR][1000 genomes]
rs7020326	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7030816	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7031850	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7032033	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7034155	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7041051	0.85[EUR][1000 genomes]
rs7043125	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7043519	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7849732	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7849944	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7851440	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7858895	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7864726	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1046590	chr9:104450624-104848588	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1046614	chr9:104492314-104686326	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1054992	chr9:104494816-104771134	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1043967	chr9:104498664-104636328	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104501200-104502400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
2	chr9:104501400-104502400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
3	chr9:104501400-104502600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
4	chr9:104501400-104502800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr9:104501600-104503400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:104501800-104502800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr9:104502000-104502600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr9:104502200-104503000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr9:104502200-104503000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell

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