Variant report

Variant	rs7302629
Chromosome Location	chr12:86024749-86024750
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 123 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10083104	0.85[EUR][1000 genomes]
rs10466964	0.86[EUR][1000 genomes]
rs10746346	0.84[ASN][1000 genomes]
rs10746347	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10779161	0.81[ASN][1000 genomes]
rs10779164	0.87[ASN][1000 genomes]
rs10779167	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10779168	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10779169	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10779170	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10779173	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10779179	0.84[EUR][1000 genomes]
rs10779180	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10779181	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10779182	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10779188	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10862990	0.88[ASN][1000 genomes]
rs10862991	0.87[ASN][1000 genomes]
rs10862993	0.87[ASN][1000 genomes]
rs10862999	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10863000	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10863007	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10863008	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10863022	0.87[EUR][1000 genomes]
rs10863023	0.81[EUR][1000 genomes]
rs10863031	0.85[EUR][1000 genomes]
rs10863032	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10863034	0.84[EUR][1000 genomes]
rs11116832	0.83[ASN][1000 genomes]
rs11116833	0.83[ASN][1000 genomes]
rs11116913	0.82[EUR][1000 genomes]
rs11116930	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11116934	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11116935	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11116945	0.85[EUR][1000 genomes]
rs11116965	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11116966	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11116967	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11116968	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11116969	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11831266	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11835161	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12303708	0.82[EUR][1000 genomes]
rs12308693	0.84[EUR][1000 genomes]
rs12308694	0.84[EUR][1000 genomes]
rs12578708	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1398442	0.82[ASN][1000 genomes]
rs17013043	0.87[EUR][1000 genomes]
rs1870933	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1870935	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2199506	0.84[EUR][1000 genomes]
rs2199508	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2199510	0.81[EUR][1000 genomes]
rs2199511	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2199512	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2199513	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2199516	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2199517	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2199518	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2219711	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2405248	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2405254	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2405256	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2405257	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2405260	0.84[EUR][1000 genomes]
rs28637596	0.87[EUR][1000 genomes]
rs2897092	0.85[EUR][1000 genomes]
rs34750736	0.84[EUR][1000 genomes]
rs4143506	0.82[EUR][1000 genomes]
rs4761063	0.84[ASN][1000 genomes]
rs4897817	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4897825	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4897842	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4897843	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6419420	0.82[ASN][1000 genomes]
rs6419421	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6539899	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6539901	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6539902	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7133064	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7133855	0.88[ASN][1000 genomes]
rs7134486	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7136236	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7295445	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7297262	0.88[ASN][1000 genomes]
rs7300800	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7300819	0.85[EUR][1000 genomes]
rs7303316	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7304475	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7308482	0.87[EUR][1000 genomes]
rs7310496	0.87[EUR][1000 genomes]
rs7316167	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7485084	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7485590	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7486767	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7487599	0.82[ASN][1000 genomes]
rs7955601	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7957797	0.84[ASN][1000 genomes]
rs7966898	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7973153	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7973323	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7977259	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs898986	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9788015	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9788074	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817242	chr12:85622245-86069213	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1054573	chr12:85658602-86235433	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1035600	chr12:85661373-86235433	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv2751125	chr12:85884858-86098240	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1043253	chr12:85888151-86125364	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1037938	chr12:85902517-86045125	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2761758	chr12:85906092-86045137	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv455679	chr12:85908396-86024749	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv559664	chr12:85908396-86024749	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv559665	chr12:85908396-86070692	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	esv2751126	chr12:85912432-86061403	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv1052187	chr12:85954455-86278200	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv541560	chr12:85954455-86278200	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	nsv1054475	chr12:85985510-86175711	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv541561	chr12:85985510-86175711	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv430522	chr12:86010755-86069542	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	nsv1042467	chr12:86017619-86078149	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
18	nsv522439	chr12:86020998-86066266	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7302629	NTS	cis	lymphoblastoid	seeQTL
rs7302629	RASSF9	cis	Esophagus Mucosa	GTEx

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86021600-86026200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:86021800-86025800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:86021800-86025800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:86021800-86026000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:86021800-86027200	Weak transcription	NHDF-Ad	bronchial
6	chr12:86022000-86026000	Weak transcription	Hela-S3	cervix
7	chr12:86022000-86026000	Weak transcription	HUVEC	blood vessel
8	chr12:86024000-86024800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:86024400-86025000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:86024600-86026600	Enhancers	NHEK	skin

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