Variant report

Variant	rs62576500
Chromosome Location	chr9:118236551-118236552
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12002475	0.81[ASN][1000 genomes]
rs12003493	0.81[ASN][1000 genomes]
rs1335142	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62576480	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62576482	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62576499	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62576501	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62576502	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62576506	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62576528	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62576529	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62576530	0.80[EUR][1000 genomes]
rs62576532	0.80[EUR][1000 genomes]
rs62576534	0.80[EUR][1000 genomes]
rs62576537	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62576538	0.81[ASN][1000 genomes]
rs62576539	0.81[ASN][1000 genomes]
rs62576662	0.81[ASN][1000 genomes]
rs62576663	0.81[ASN][1000 genomes]
rs62576664	0.81[ASN][1000 genomes]
rs62576666	0.81[ASN][1000 genomes]
rs62577508	0.82[EUR][1000 genomes]
rs62577526	0.81[EUR][1000 genomes]
rs62577528	0.82[EUR][1000 genomes]
rs62577529	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62577532	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72750117	0.83[EUR][1000 genomes]
rs72755374	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs959486	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv948346	chr9:118107565-118718197	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1042957	chr9:118153824-118313540	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1046948	chr9:118185587-118926891	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv916622	chr9:118206309-118952390	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv540207	chr9:118206311-118920304	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv491661	chr9:118206312-118802177	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv893770	chr9:118213502-118299750	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118235000-118239400	Active TSS	H9 Cell Line	embryonic stem cell
2	chr9:118235200-118238200	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr9:118235200-118238400	Active TSS	H1 Cell Line	embryonic stem cell
4	chr9:118235400-118236600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr9:118235400-118236800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
6	chr9:118235400-118237000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr9:118235400-118237600	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr9:118235400-118238200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:118235400-118238400	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr9:118235400-118239200	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr9:118235600-118238200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr9:118236200-118237000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:118236200-118237600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:118236200-118237800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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