Variant report

Variant	rs10468217
Chromosome Location	chr15:83248079-83248080
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10400906	0.90[ASN][1000 genomes]
rs10906984	0.87[ASN][1000 genomes]
rs1145172	0.92[ASN][1000 genomes]
rs1145173	0.92[ASN][1000 genomes]
rs11631963	0.84[ASN][1000 genomes]
rs11633829	0.90[ASN][1000 genomes]
rs11635624	0.81[ASN][1000 genomes]
rs11637433	0.92[ASN][1000 genomes]
rs11855735	0.89[ASN][1000 genomes]
rs12148332	0.94[ASN][1000 genomes]
rs12438312	0.87[ASN][1000 genomes]
rs12442686	0.85[ASN][1000 genomes]
rs1259180	0.98[ASN][1000 genomes]
rs1259182	0.91[ASN][1000 genomes]
rs1259183	0.88[ASN][1000 genomes]
rs1267657	0.94[ASN][1000 genomes]
rs1267658	0.93[ASN][1000 genomes]
rs1267659	0.93[ASN][1000 genomes]
rs1269134	0.90[ASN][1000 genomes]
rs12911134	0.84[ASN][1000 genomes]
rs12916980	0.92[ASN][1000 genomes]
rs1313492	0.93[ASN][1000 genomes]
rs1313493	0.93[ASN][1000 genomes]
rs1367841	0.92[ASN][1000 genomes]
rs1594511	0.92[ASN][1000 genomes]
rs17158390	0.91[ASN][1000 genomes]
rs1864699	0.92[ASN][1000 genomes]
rs2099259	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2278355	0.87[ASN][1000 genomes]
rs2567635	0.94[ASN][1000 genomes]
rs2567636	0.94[ASN][1000 genomes]
rs2678445	0.94[ASN][1000 genomes]
rs2678448	0.94[ASN][1000 genomes]
rs28374463	0.87[ASN][1000 genomes]
rs28415133	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28667458	0.84[ASN][1000 genomes]
rs2870965	0.87[ASN][1000 genomes]
rs2870966	0.91[ASN][1000 genomes]
rs28808991	0.95[ASN][1000 genomes]
rs34186444	0.91[ASN][1000 genomes]
rs35934048	0.95[ASN][1000 genomes]
rs36109438	0.93[ASN][1000 genomes]
rs3970696	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4778686	0.92[ASN][1000 genomes]
rs4779032	0.98[ASN][1000 genomes]
rs4779039	0.84[ASN][1000 genomes]
rs4779041	0.92[ASN][1000 genomes]
rs4779044	0.90[ASN][1000 genomes]
rs4779050	0.87[ASN][1000 genomes]
rs4779053	0.84[ASN][1000 genomes]
rs55924160	0.91[ASN][1000 genomes]
rs57181760	0.90[ASN][1000 genomes]
rs62009923	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6603033	0.92[ASN][1000 genomes]
rs698500	0.96[ASN][1000 genomes]
rs7165125	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7166248	0.84[ASN][1000 genomes]
rs7167880	0.91[ASN][1000 genomes]
rs7171180	0.92[ASN][1000 genomes]
rs7178350	0.88[ASN][1000 genomes]
rs7181761	0.84[ASN][1000 genomes]
rs7182403	0.90[ASN][1000 genomes]
rs7183881	0.90[ASN][1000 genomes]
rs7494860	0.92[ASN][1000 genomes]
rs7496954	0.90[ASN][1000 genomes]
rs783520	0.90[ASN][1000 genomes]
rs783521	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs783522	0.80[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs783523	0.91[ASN][1000 genomes]
rs783525	0.91[ASN][1000 genomes]
rs783526	0.92[ASN][1000 genomes]
rs783527	0.90[ASN][1000 genomes]
rs783529	0.94[ASN][1000 genomes]
rs783530	0.94[ASN][1000 genomes]
rs783531	0.99[ASN][1000 genomes]
rs783532	0.97[ASN][1000 genomes]
rs783533	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs783534	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs783535	0.93[ASN][1000 genomes]
rs783536	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs783537	0.92[ASN][1000 genomes]
rs783539	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs783540	0.95[ASN][1000 genomes]
rs783543	0.91[ASN][1000 genomes]
rs783545	0.97[ASN][1000 genomes]
rs803687	0.91[ASN][1000 genomes]
rs803688	0.92[ASN][1000 genomes]
rs803747	0.95[ASN][1000 genomes]
rs8040293	0.88[ASN][1000 genomes]
rs8043401	0.88[ASN][1000 genomes]
rs9652567	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427965	chr15:82741381-83310525	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv428309	chr15:82741381-83310525	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv2758391	chr15:82879646-83310525	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	esv2760046	chr15:82879646-83310525	Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv1035899	chr15:83108446-83315731	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv833071	chr15:83123646-83310510	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1054171	chr15:83237514-83468077	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
8	nsv1036950	chr15:83245326-83461261	Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
9	nsv1036462	chr15:83245326-83472507	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs10468217	RP13-996F3.5	cis	Esophagus Mucosa	GTEx
rs10468217	GOLGA6L10	cis	Esophagus Mucosa	GTEx
rs10468217	FLJ40113///LOC161527///LOC440295///LOC642346	N/A	lymphoblastoid	RTeQTL
rs10468217	GOLGA6L10	cis	Esophagus Muscularis	GTEx
rs10468217	LOC402057///RPS17	trans	lymphoblastoid	RTeQTL
rs10468217	RPS17	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:83241400-83248400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:83241800-83297600	Weak transcription	Brain Inferior Temporal Lobe	brain

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