Variant report

Variant	rs10756632
Chromosome Location	chr9:14987263-14987264
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10114147	0.84[EUR][1000 genomes]
rs10511603	0.88[ASN][1000 genomes]
rs10511604	0.82[ASN][1000 genomes]
rs10756635	0.88[ASN][1000 genomes]
rs10756636	0.88[ASN][1000 genomes]
rs10756637	0.88[ASN][1000 genomes]
rs10810297	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10810298	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10810307	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10810308	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10810309	1.00[ASN][1000 genomes]
rs10810310	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10810311	0.94[ASN][1000 genomes]
rs10810312	0.94[ASN][1000 genomes]
rs10810314	0.90[ASN][1000 genomes]
rs10810315	0.89[ASN][1000 genomes]
rs10810316	0.88[ASN][1000 genomes]
rs10810317	0.88[ASN][1000 genomes]
rs10810318	0.82[ASN][1000 genomes]
rs10810319	0.81[ASN][1000 genomes]
rs10810320	0.88[ASN][1000 genomes]
rs10810321	0.88[ASN][1000 genomes]
rs10810323	0.88[ASN][1000 genomes]
rs10810326	0.88[ASN][1000 genomes]
rs10810327	0.88[ASN][1000 genomes]
rs10961817	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10961819	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10961820	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10961825	0.91[ASN][1000 genomes]
rs10961826	0.91[ASN][1000 genomes]
rs10961827	0.88[ASN][1000 genomes]
rs10961828	0.88[ASN][1000 genomes]
rs10961831	0.88[ASN][1000 genomes]
rs10961832	0.88[ASN][1000 genomes]
rs11788817	0.88[ASN][1000 genomes]
rs11793253	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12335682	0.94[ASN][1000 genomes]
rs12340301	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12343244	0.83[ASN][1000 genomes]
rs12344181	0.83[ASN][1000 genomes]
rs12352024	0.85[ASN][1000 genomes]
rs12379705	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1357474	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1412720	0.85[EUR][1000 genomes]
rs1464608	0.85[EUR][1000 genomes]
rs1589666	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17223865	0.83[ASN][1000 genomes]
rs1829850	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1851588	0.90[ASN][1000 genomes]
rs1851590	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1880012	0.84[EUR][1000 genomes]
rs1880013	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1916311	0.88[ASN][1000 genomes]
rs1916312	0.88[ASN][1000 genomes]
rs1916313	0.83[ASN][1000 genomes]
rs2011091	0.88[ASN][1000 genomes]
rs2049291	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2140322	0.83[EUR][1000 genomes]
rs2381973	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2382508	0.83[ASN][1000 genomes]
rs4008009	0.83[EUR][1000 genomes]
rs4535838	0.83[EUR][1000 genomes]
rs4548277	0.84[EUR][1000 genomes]
rs4553007	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57255198	0.88[ASN][1000 genomes]
rs62536769	0.91[ASN][1000 genomes]
rs6474876	0.85[EUR][1000 genomes]
rs6474878	0.81[EUR][1000 genomes]
rs7018678	0.84[EUR][1000 genomes]
rs7020107	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7026072	0.84[EUR][1000 genomes]
rs7028104	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7028135	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7028702	0.91[EUR][1000 genomes]
rs7030516	0.84[EUR][1000 genomes]
rs7037967	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs7040712	0.84[EUR][1000 genomes]
rs7042782	0.87[EUR][1000 genomes]
rs7046824	0.82[EUR][1000 genomes]
rs7048509	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7350286	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7350287	0.85[EUR][1000 genomes]
rs7848747	0.83[EUR][1000 genomes]
rs7855093	0.86[EUR][1000 genomes]
rs7858719	0.88[ASN][1000 genomes]
rs7858723	0.88[ASN][1000 genomes]
rs9298710	0.84[EUR][1000 genomes]
rs940118	0.88[ASN][1000 genomes]
rs9886740	0.88[ASN][1000 genomes]
rs9886864	0.88[ASN][1000 genomes]
rs9886867	0.88[ASN][1000 genomes]
rs9886868	0.88[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	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv892620	chr9:14922877-15086021	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv892621	chr9:14928013-15043692	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2761503	chr9:14960217-15049343	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv892622	chr9:14960217-15055607	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10756632	RP11-54D18.2	cis	Esophagus Muscularis	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14973800-14991400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr9:14981000-14992400	Weak transcription	Fetal Heart	heart
3	chr9:14982200-14992600	Weak transcription	Fetal Lung	lung
4	chr9:14982400-14988800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:14982600-14992000	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:14987200-14992400	Weak transcription	H1 Cell Line	embryonic stem cell

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