Variant report

Variant	rs8007946
Chromosome Location	chr14:31935173-31935174
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:31925030..31927583-chr14:31933327..31936225,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129480	Chromatin interaction
ENSG00000203546	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10134812	1.00[EUR][1000 genomes]
rs10138925	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10147284	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10150938	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10151479	0.97[EUR][1000 genomes]
rs11156673	0.91[EUR][1000 genomes]
rs11620714	0.90[EUR][1000 genomes]
rs11624231	0.89[ASN][1000 genomes]
rs11845550	0.93[EUR][1000 genomes]
rs11845830	0.93[EUR][1000 genomes]
rs11846073	0.81[EUR][1000 genomes]
rs11847017	0.94[EUR][1000 genomes]
rs11847614	0.94[EUR][1000 genomes]
rs11850265	0.94[EUR][1000 genomes]
rs11850273	0.94[EUR][1000 genomes]
rs11851140	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12436396	0.91[EUR][1000 genomes]
rs12590885	0.91[EUR][1000 genomes]
rs12881016	0.93[EUR][1000 genomes]
rs12881925	0.96[EUR][1000 genomes]
rs12891556	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12891787	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12892435	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13176	0.93[EUR][1000 genomes]
rs17097881	0.89[ASN][1000 genomes]
rs17097892	0.95[ASN][1000 genomes]
rs17097896	0.94[ASN][1000 genomes]
rs17097898	0.92[ASN][1000 genomes]
rs1958027	0.91[EUR][1000 genomes]
rs2094906	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2182254	0.94[EUR][1000 genomes]
rs2274291	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34182758	0.90[EUR][1000 genomes]
rs34278949	0.89[EUR][1000 genomes]
rs34704647	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35483550	0.92[EUR][1000 genomes]
rs4981100	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4981101	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4981849	0.97[EUR][1000 genomes]
rs4981850	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4981851	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5016597	0.95[EUR][1000 genomes]
rs55864289	0.95[ASN][1000 genomes]
rs56183134	0.94[ASN][1000 genomes]
rs6571423	0.90[EUR][1000 genomes]
rs6571426	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7149165	0.93[EUR][1000 genomes]
rs7149522	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7153450	0.93[EUR][1000 genomes]
rs7154915	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7157390	0.93[EUR][1000 genomes]
rs7159566	0.85[EUR][1000 genomes]
rs8006990	0.98[EUR][1000 genomes]
rs8007488	0.96[EUR][1000 genomes]
rs8008016	0.96[EUR][1000 genomes]
rs8010209	0.88[EUR][1000 genomes]
rs8011206	0.93[EUR][1000 genomes]
rs8012658	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv901589	chr14:31768231-31944723	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1042776	chr14:31844026-32003929	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv542019	chr14:31844026-32003929	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv931935	chr14:31871658-32117666	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv1050774	chr14:31879687-32102906	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv934110	chr14:31887749-32109529	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv934206	chr14:31887749-32257097	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
9	nsv456198	chr14:31919728-31972289	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv564179	chr14:31919728-31972289	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS 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
rs8007946	C14orf126	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31927200-31939000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:31927800-31939400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:31934000-31936400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr14:31934200-31935200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:31934800-31936200	Enhancers	Adipose Nuclei	Adipose

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