Variant report

Variant	rs2184064
Chromosome Location	chr1:160887475-160887476
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:160850486..160853249-chr1:160886390..160887944,2	K562	blood:

Variant related genes	Relation type
ENSG00000179914	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10797087	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10797089	0.85[EUR][1000 genomes]
rs10908809	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10908810	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10908811	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10908812	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10908813	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1092415	0.92[ASN][1000 genomes]
rs11265510	0.88[EUR][1000 genomes]
rs11265514	0.91[EUR][1000 genomes]
rs11265516	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11265519	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11587040	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12080285	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12125065	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12135639	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12740520	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1810924	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1855186	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1855187	0.88[EUR][1000 genomes]
rs1930596	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1930598	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2039415	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2225591	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2297559	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34295669	0.88[EUR][1000 genomes]
rs3953093	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3953095	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4017453	0.88[EUR][1000 genomes]
rs4129196	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4656277	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4656282	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4656958	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4656959	0.88[EUR][1000 genomes]
rs4656964	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6427559	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6674437	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6691868	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6694415	0.86[EUR][1000 genomes]
rs6694743	0.83[EUR][1000 genomes]
rs6704490	0.86[EUR][1000 genomes]
rs7414826	0.89[EUR][1000 genomes]
rs7551697	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530077	chr1:160836448-161284904	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	esv3430322	chr1:160851829-160920480	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv947200	chr1:160870136-160905390	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2184064	RP11-312J18.6	cis	Thyroid	GTEx

Chromatin state (count:0 , 50 per page) page:

No data

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