Variant report

Variant	rs4580302
Chromosome Location	chr19:44554049-44554050
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11083736	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11083737	0.82[ASN][1000 genomes]
rs12610472	0.82[ASN][1000 genomes]
rs2138823	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2138824	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2176431	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35120085	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3826941	0.82[ASN][1000 genomes]
rs4239528	0.82[ASN][1000 genomes]
rs4299256	0.81[ASN][1000 genomes]
rs4371266	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4375771	0.82[ASN][1000 genomes]
rs4444434	0.82[ASN][1000 genomes]
rs4550576	0.81[ASN][1000 genomes]
rs4555257	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4803668	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4803672	0.87[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs55798868	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs56003307	0.84[ASN][1000 genomes]
rs56230322	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs56250154	0.84[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs57895932	0.81[ASN][1000 genomes]
rs62119177	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6509135	0.83[ASN][1000 genomes]
rs6509137	0.82[ASN][1000 genomes]
rs7251015	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7252213	0.81[ASN][1000 genomes]
rs7255192	0.84[ASN][1000 genomes]
rs8105003	0.81[ASN][1000 genomes]
rs8109313	0.82[ASN][1000 genomes]
rs8109615	0.85[ASN][1000 genomes]
rs8110348	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9646633	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469650	chr19:44405994-44555426	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv833840	chr19:44520620-44715760	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4580302	ZNF223	cis	lung	GTEx
rs4580302	ZNF223	cis	Thyroid	GTEx
rs4580302	ZNF223	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44553600-44555200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr19:44553800-44554600	Weak transcription	Psoas Muscle	Psoas

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