Variant report

Variant	rs12237438
Chromosome Location	chr9:99919913-99919914
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10817175	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10817176	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817177	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817178	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10817179	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10817180	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10817181	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10817183	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10817192	0.91[EUR][1000 genomes]
rs10817211	0.88[EUR][1000 genomes]
rs10980872	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10980873	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10980889	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10980894	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10980896	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10980912	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10980939	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10981026	0.91[EUR][1000 genomes]
rs10981130	0.87[EUR][1000 genomes]
rs11789331	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11792076	0.92[EUR][1000 genomes]
rs11792723	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11792736	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11794757	0.81[EUR][1000 genomes]
rs11795173	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12235225	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12235677	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12237712	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12237849	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12238318	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12238745	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1986463	0.91[EUR][1000 genomes]
rs3953684	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41281914	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4263876	0.91[EUR][1000 genomes]
rs56722769	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57176573	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57936136	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58723976	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61050463	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7032137	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73654680	0.91[EUR][1000 genomes]
rs7873111	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831662	chr9:99752521-99939231	Bivalent Enhancer Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv972432	chr9:99874607-99958095	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv931946	chr9:99895658-100005099	Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv893607	chr9:99906545-99996548	Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893608	chr9:99906545-100005128	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS 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	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99901000-99921000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:99909800-99920200	Weak transcription	Brain Angular Gyrus	brain
3	chr9:99911600-99957600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:99912200-99921200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:99912200-99922800	Weak transcription	Brain Anterior Caudate	brain
6	chr9:99912200-99923800	Strong transcription	H1 Cell Line	embryonic stem cell
7	chr9:99913000-99920000	Strong transcription	H9 Cell Line	embryonic stem cell
8	chr9:99913000-99924400	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr9:99913200-99923600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
10	chr9:99913200-99924200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:99913400-99924600	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:99913400-99930800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr9:99913600-99924200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr9:99913600-99930800	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr9:99916800-99921800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:99918000-99946800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:99918400-99921000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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