Variant report

Variant	rs17138834
Chromosome Location	chr5:115412322-115412323
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:115410908..115413272-chr5:115413402..115416355,3	MCF-7	breast:
2	chr5:115409968..115416849-chr5:115417165..115422986,15	K562	blood:
3	chr5:115412238..115416929-chr5:115418524..115421820,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272265	Chromatin interaction
ENSG00000145781	Chromatin interaction
ENSG00000271918	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs1001014	0.85[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap]
rs10051047	0.85[CHB][hapmap]
rs10059969	0.85[CHB][hapmap]
rs10059989	0.84[CHB][hapmap]
rs10068730	0.85[CHB][hapmap]
rs10069565	0.85[CHB][hapmap]
rs10071359	0.85[CHB][hapmap]
rs10073199	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs10074746	0.85[CHB][hapmap]
rs10076543	0.85[CHB][hapmap]
rs10076661	0.84[CHB][hapmap]
rs10077113	0.91[CHB][hapmap]
rs10477550	0.85[CHB][hapmap]
rs10478286	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs10478287	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs10519444	1.00[CHB][hapmap];0.90[CHD][hapmap];0.85[GIH][hapmap];0.91[JPT][hapmap]
rs11241379	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1129495	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11951682	0.84[CHB][hapmap]
rs11954350	0.85[CHB][hapmap]
rs11955144	0.85[CHB][hapmap]
rs11955906	0.85[CHB][hapmap]
rs11957382	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs11958647	0.92[CHB][hapmap]
rs12522977	0.84[CHB][hapmap]
rs13362436	1.00[CHB][hapmap];0.90[CHD][hapmap];0.91[JPT][hapmap]
rs1396484	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs1396486	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs1508870	0.84[CHB][hapmap]
rs1508873	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs1543952	0.85[CHB][hapmap]
rs1567330	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1567331	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1567332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1567338	0.85[CHB][hapmap]
rs1567339	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs17138841	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17138848	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17138850	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17138853	0.90[JPT][hapmap]
rs17138861	0.85[CHB][hapmap]
rs17138866	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17138879	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.92[TSI][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17138925	0.90[JPT][hapmap]
rs17139182	0.90[JPT][hapmap]
rs17139253	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap]
rs17139333	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];0.85[TSI][hapmap]
rs1876672	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs1876676	0.85[CHB][hapmap]
rs2136213	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap];0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2136214	0.90[JPT][hapmap]
rs2161321	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs2174996	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs2416434	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs3087831	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3087832	1.00[CEU][hapmap];0.88[YRI][hapmap];0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3946989	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4260709	0.91[CHB][hapmap]
rs4301260	0.85[CHB][hapmap]
rs4484468	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs4507525	0.83[CHB][hapmap]
rs4593303	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs4921058	0.86[ASN][1000 genomes]
rs4921060	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4921071	0.85[CEU][hapmap];0.88[CHB][hapmap]
rs4921076	0.85[CHB][hapmap]
rs4921078	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs4921085	0.85[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap]
rs56953556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57697861	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58172625	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58510083	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59429923	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61105089	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61632432	0.87[AFR][1000 genomes]
rs61672521	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6859670	0.85[CHB][hapmap]
rs6860662	0.82[LWK][hapmap]
rs6874458	0.85[CHB][hapmap]
rs6874747	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs6876214	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap]
rs6878530	0.85[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.80[MKK][hapmap];0.85[TSI][hapmap]
rs6878871	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs6879075	0.85[CHB][hapmap]
rs6882942	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6887275	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs6887852	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs6888823	0.85[CEU][hapmap];0.91[JPT][hapmap]
rs6890263	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6894471	0.85[CHB][hapmap]
rs6898524	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs73271268	0.84[ASN][1000 genomes]
rs73780832	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7449449	0.85[CHB][hapmap]
rs7701736	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs7702152	1.00[CHB][hapmap]
rs7703978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7707191	0.85[CHB][hapmap]
rs7718843	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs7719318	0.85[CHB][hapmap]
rs7720518	0.84[CHB][hapmap]
rs7721510	0.85[CHB][hapmap]
rs7723648	0.85[CHB][hapmap]
rs7726794	1.00[CHB][hapmap]
rs7728055	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7730943	0.85[CHB][hapmap]
rs7733187	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap]
rs7734614	0.85[CHB][hapmap]
rs7736793	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.80[MKK][hapmap];0.85[TSI][hapmap]
rs9326997	0.85[CHB][hapmap]
rs9686231	0.85[CHB][hapmap];0.80[CHD][hapmap]
rs9686686	0.85[CHB][hapmap]
rs9687350	0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949677	chr5:115104829-115496168	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1027418	chr5:115206256-115446861	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv515611	chr5:115208843-115428381	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1021968	chr5:115213162-115426468	Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv1024008	chr5:115222974-115431050	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv1027117	chr5:115222974-115442883	Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	esv2763487	chr5:115222986-115442895	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv462400	chr5:115223504-115428381	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv599478	chr5:115223504-115428381	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv1030480	chr5:115228889-115446861	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
11	nsv599479	chr5:115233116-115450969	ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	nsv1015976	chr5:115236239-115434163	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv537868	chr5:115236239-115434163	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
14	nsv882736	chr5:115254723-115552945	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
15	nsv882737	chr5:115263853-115552945	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
16	esv34146	chr5:115315944-115729919	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	nsv527320	chr5:115382097-115573543	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv1027266	chr5:115382704-115501792	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
19	esv2755349	chr5:115384101-115733101	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
20	nsv1032199	chr5:115384131-115525738	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
21	esv2830404	chr5:115386661-115490546	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS 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
22	nsv1019972	chr5:115386860-115563533	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
23	nsv537869	chr5:115386860-115563533	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
24	nsv1018861	chr5:115397834-115563533	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
25	nsv537870	chr5:115397834-115563533	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17138834	COMMD10	cis	lymphoblastoid	seeQTL

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115405400-115419600	Weak transcription	Fetal Brain Male	brain
2	chr5:115410600-115419400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:115410800-115413200	Enhancers	Primary B cells from peripheral blood	blood
4	chr5:115411000-115413200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:115411000-115419600	Weak transcription	Fetal Intestine Small	intestine
6	chr5:115411000-115419600	Weak transcription	Pancreas	Pancrea
7	chr5:115411200-115412600	Enhancers	GM12878-XiMat	blood
8	chr5:115411400-115413400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr5:115411400-115419600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:115411600-115413000	Enhancers	Primary B cells from cord blood	blood
11	chr5:115411600-115413000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:115411600-115413200	Enhancers	Primary hematopoietic stem cells	blood
13	chr5:115411600-115413400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr5:115411600-115419400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr5:115411600-115419400	Weak transcription	K562	blood
16	chr5:115411600-115419600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr5:115412000-115412400	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr5:115412200-115413000	Enhancers	Primary T helper cells PMA-I stimulated	--

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