Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11584680	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12749731	0.81[ASN][1000 genomes]
rs16854042	0.90[ASN][1000 genomes]
rs4072451	0.88[ASN][1000 genomes]
rs4072452	0.90[ASN][1000 genomes]
rs4111171	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4651029	0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4651030	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4652400	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56232973	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59559400	0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6425542	0.81[ASN][1000 genomes]
rs6425543	0.81[ASN][1000 genomes]
rs6425557	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6656056	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6657452	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6665787	0.88[ASN][1000 genomes]
rs6690348	0.81[ASN][1000 genomes]
rs6693527	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6698526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72704417	0.86[EUR][1000 genomes]
rs72719243	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7521291	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs962428	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9660976	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3514400	chr1:179349344-179400533	Enhancers Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3514401	chr1:179349344-179400533	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3451112	chr1:179352344-179400533	Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1819329	chr1:179371973-179442337	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv466217	chr1:179371973-179477921	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv548297	chr1:179371973-179477921	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv548298	chr1:179376896-179436288	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs9726734	TDRD5	cis	Esophagus Mucosa	GTEx
rs9726734	TDRD5	cis	lung	GTEx
rs9726734	TDRD5	cis	Thyroid	GTEx
rs9726734	TDRD5	cis	Nerve Tibial	GTEx
rs9726734	TDRD5	cis	Artery Tibial	GTEx
rs9726734	TDRD5	cis	Adipose Subcutaneous	GTEx
rs9726734	TDRD5	cis	Artery Aorta	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179391600-179394800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:179394600-179394800	Enhancers	iPS-20b Cell Line	embryonic stem cell

Quick Search: