Variant report

Variant	rs7861033
Chromosome Location	chr9:118618694-118618695
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10448252	0.98[EUR][1000 genomes]
rs10759826	0.87[EUR][1000 genomes]
rs10817838	1.00[EUR][1000 genomes]
rs10982941	0.81[EUR][1000 genomes]
rs10982942	0.81[EUR][1000 genomes]
rs10982943	0.87[EUR][1000 genomes]
rs10982952	0.98[EUR][1000 genomes]
rs10982953	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10982957	1.00[EUR][1000 genomes]
rs10982967	0.85[EUR][1000 genomes]
rs10982968	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10982970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10982976	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982978	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982979	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982981	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982982	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982983	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982984	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982985	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10982988	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10982991	0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs10982996	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10982997	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs10982998	0.85[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs10983000	0.85[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10983003	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10983004	0.85[CHB][hapmap];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10983005	0.85[CHB][hapmap];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10983007	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12156496	0.81[EUR][1000 genomes]
rs12378638	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12378736	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12380105	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1243	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2040485	0.85[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2418420	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2418424	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3761841	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3789264	0.85[CHB][hapmap];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4145478	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62575660	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62575661	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62575662	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62575663	0.90[ASN][1000 genomes]
rs62575664	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62575665	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62577089	0.81[EUR][1000 genomes]
rs62577094	0.81[EUR][1000 genomes]
rs62577095	0.98[EUR][1000 genomes]
rs62577110	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62577130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62577137	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62577138	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577139	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577140	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577141	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577142	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577143	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577146	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577147	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577148	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62577150	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62577151	0.85[EUR][1000 genomes]
rs62577152	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs68019277	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7024074	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7029447	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7046862	1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7047141	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616610	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616612	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616613	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616614	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616615	0.85[EUR][1000 genomes];0.90[ASN][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	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
2	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
3	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
4	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
5	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
6	nsv831699	chr9:118457011-118641819	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118617600-118619000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr9:118617600-118619200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr9:118617600-118619200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:118617600-118619200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:118618600-118619400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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