Variant report

Variant	rs10147284
Chromosome Location	chr14:31945282-31945283
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10134812	0.99[EUR][1000 genomes]
rs10138925	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10150938	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10151479	0.96[EUR][1000 genomes]
rs11156673	0.90[EUR][1000 genomes]
rs11620714	0.89[EUR][1000 genomes]
rs11624231	0.89[ASN][1000 genomes]
rs11845550	0.92[EUR][1000 genomes]
rs11845830	0.92[EUR][1000 genomes]
rs11846073	0.80[EUR][1000 genomes]
rs11847017	0.95[EUR][1000 genomes]
rs11847614	0.93[EUR][1000 genomes]
rs11850265	0.93[EUR][1000 genomes]
rs11850273	0.93[EUR][1000 genomes]
rs11851140	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12436396	0.90[EUR][1000 genomes]
rs12590885	0.90[EUR][1000 genomes]
rs12881016	0.92[EUR][1000 genomes]
rs12881925	0.97[EUR][1000 genomes]
rs12891556	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12891787	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12892435	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13176	0.92[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	0.90[EUR][1000 genomes]
rs2094906	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2104820	0.80[EUR][1000 genomes]
rs2182254	0.93[EUR][1000 genomes]
rs2274291	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34182758	0.89[EUR][1000 genomes]
rs34278949	0.88[EUR][1000 genomes]
rs34704647	0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35483550	0.91[EUR][1000 genomes]
rs4981100	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4981101	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4981849	0.98[EUR][1000 genomes]
rs4981850	0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4981851	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5016597	0.94[EUR][1000 genomes]
rs55864289	0.95[ASN][1000 genomes]
rs56183134	0.94[ASN][1000 genomes]
rs6571423	0.89[EUR][1000 genomes]
rs6571426	0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7149165	0.92[EUR][1000 genomes]
rs7149522	0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7153450	0.92[EUR][1000 genomes]
rs7154915	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7157390	0.92[EUR][1000 genomes]
rs7159566	0.86[EUR][1000 genomes]
rs8006990	0.99[EUR][1000 genomes]
rs8007488	0.97[EUR][1000 genomes]
rs8007946	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8008016	0.97[EUR][1000 genomes]
rs8010209	0.87[EUR][1000 genomes]
rs8011206	0.92[EUR][1000 genomes]
rs8012658	0.92[EUR][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	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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
rs10147284	C14orf126	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31944400-31946200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:31944600-31945800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:31945000-31947600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr14:31945200-31946600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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