Variant report

Variant	rs62001106
Chromosome Location	chr14:39924729-39924730
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10047876	0.90[ASN][1000 genomes]
rs10130181	0.85[ASN][1000 genomes]
rs10132190	0.85[ASN][1000 genomes]
rs10133746	0.88[ASN][1000 genomes]
rs10134065	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10136490	0.90[ASN][1000 genomes]
rs10136915	0.90[ASN][1000 genomes]
rs10142029	0.90[ASN][1000 genomes]
rs10143148	0.88[ASN][1000 genomes]
rs10144377	0.85[ASN][1000 genomes]
rs10145757	0.85[ASN][1000 genomes]
rs10146106	0.90[ASN][1000 genomes]
rs10146622	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10483538	0.81[ASN][1000 genomes]
rs12185014	0.88[ASN][1000 genomes]
rs12431558	0.81[ASN][1000 genomes]
rs12433987	0.85[ASN][1000 genomes]
rs17109168	0.90[ASN][1000 genomes]
rs17622868	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2103795	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2179973	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28398804	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28419351	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28454173	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28568594	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28571663	0.85[ASN][1000 genomes]
rs28704775	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28871954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2899887	0.85[ASN][1000 genomes]
rs4316662	0.85[ASN][1000 genomes]
rs4902559	0.85[ASN][1000 genomes]
rs61999073	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61999077	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61999079	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62000696	0.85[ASN][1000 genomes]
rs62000708	0.85[ASN][1000 genomes]
rs62000709	0.85[ASN][1000 genomes]
rs62000710	0.85[ASN][1000 genomes]
rs62000711	0.81[ASN][1000 genomes]
rs62000715	0.83[ASN][1000 genomes]
rs62000720	0.82[ASN][1000 genomes]
rs62015674	0.90[ASN][1000 genomes]
rs62015677	0.90[ASN][1000 genomes]
rs7146753	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7156962	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7158282	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7161482	0.90[ASN][1000 genomes]
rs8006076	0.90[ASN][1000 genomes]
rs8007036	0.90[ASN][1000 genomes]
rs9322999	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9805937	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037183	chr14:39736939-39949233	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers 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	39 gene(s)	inside rSNPs	diseases
2	nsv542048	chr14:39736939-39949233	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	esv3523177	chr14:39875036-40128325	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	esv3523178	chr14:39875036-40128325	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
5	nsv832774	chr14:39897746-40060823	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39923600-39925000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr14:39924000-39925000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr14:39924600-39926600	Weak transcription	GM12878-XiMat	blood

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