Variant report

Variant	rs7342384
Chromosome Location	chr12:49692487-49692488
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:49691342..49692923-chr12:49735601..49736627,8	MCF-7	breast:
2	chr12:49691489..49693674-chr12:49738441..49740198,2	MCF-7	breast:
3	chr12:49524142..49526154-chr12:49690463..49692891,2	MCF-7	breast:
4	chr12:49656941..49662685-chr12:49687034..49693573,13	MCF-7	breast:
5	chr12:49685493..49694205-chr12:49728829..49734805,16	K562	blood:
6	chr12:49664091..49667882-chr12:49690109..49694759,4	K562	blood:
7	chr12:49680691..49694205-chr12:49725987..49738512,25	K562	blood:
8	chr12:49691633..49692545-chr12:49750700..49751496,2	MCF-7	breast:
9	chr12:49656956..49663896-chr12:49681239..49693031,16	K562	blood:
10	chr12:49691887..49692585-chr12:49730635..49731419,3	MCF-7	breast:
11	chr12:49691968..49693557-chr12:49739868..49741612,2	MCF-7	breast:
12	chr12:49691634..49692517-chr12:49725409..49726067,4	MCF-7	breast:
13	chr12:49691373..49692810-chr12:49735826..49736936,11	MCF-7	breast:
14	chr12:49657190..49661099-chr12:49688432..49694179,9	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258232	Chromatin interaction
ENSG00000258017	Chromatin interaction
ENSG00000186897	Chromatin interaction
ENSG00000178401	Chromatin interaction
ENSG00000123416	Chromatin interaction
ENSG00000167553	Chromatin interaction
ENSG00000258101	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10506284	1.00[CHB][hapmap]
rs10875948	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11168967	0.87[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.90[TSI][hapmap];0.86[YRI][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11168970	0.81[AMR][1000 genomes]
rs11168973	0.93[CEU][hapmap]
rs11168975	1.00[JPT][hapmap]
rs11169016	1.00[CHB][hapmap]
rs11834161	1.00[CHB][hapmap]
rs11835037	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11835303	1.00[JPT][hapmap]
rs11837234	0.80[ASW][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12301545	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12301632	1.00[CHB][hapmap]
rs12304800	0.86[AMR][1000 genomes]
rs12306118	1.00[CHB][hapmap]
rs12313435	0.86[AMR][1000 genomes]
rs12315095	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12315130	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12315996	1.00[CHB][hapmap]
rs12317532	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12318618	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs12322335	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12322783	0.93[CEU][hapmap];0.93[MEX][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs12322798	0.83[AMR][1000 genomes]
rs12580931	0.82[CEU][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs12581343	1.00[CHB][hapmap]
rs12581428	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2070760	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2236746	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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2272478	1.00[CHB][hapmap]
rs28493849	0.82[EUR][1000 genomes]
rs28543370	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28798494	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28808573	0.82[AMR][1000 genomes]
rs28823960	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28857010	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3088008	1.00[JPT][hapmap]
rs3847764	1.00[CHB][hapmap]
rs4243545	1.00[JPT][hapmap]
rs4898516	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4898519	1.00[JPT][hapmap]
rs61023481	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61455481	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6580707	1.00[CHB][hapmap]
rs6580709	1.00[CHB][hapmap]
rs6580716	1.00[CHB][hapmap]
rs67309388	0.83[AMR][1000 genomes]
rs7136538	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7136945	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7139061	1.00[CHB][hapmap]
rs7294648	1.00[CHB][hapmap]
rs7294873	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7294973	1.00[CHB][hapmap]
rs7295162	1.00[CHB][hapmap]
rs7295247	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7309997	1.00[CHB][hapmap]
rs73112143	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7342318	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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7342365	1.00[CHB][hapmap]
rs7342370	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7955541	1.00[CHB][hapmap]
rs7962951	1.00[CHB][hapmap]
rs7969099	1.00[CHB][hapmap]
rs7975431	0.86[AMR][1000 genomes]
rs7976165	1.00[CHB][hapmap]

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	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
2	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv1036452	chr12:49376285-49867760	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	315 gene(s)	inside rSNPs	diseases
4	nsv428801	chr12:49536659-49744884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
5	nsv1042122	chr12:49678529-49823168	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1039176	chr12:49678529-49832618	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7342384	CXorf26	trans	cerebellum	SCAN
rs7342384	PRPH	cis	cerebellum	SCAN
rs7342384	TMEM117	cis	cerebellum	SCAN
rs7342384	MCRS1	cis	cerebellum	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49689600-49692600	Bivalent Enhancer	Stomach Mucosa	stomach
2	chr12:49691200-49692800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:49691600-49692600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:49691600-49692600	Enhancers	K562	blood
5	chr12:49691800-49692800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:49692200-49692600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
7	chr12:49692400-49692600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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