Variant report

Variant	rs12055227
Chromosome Location	chr5:2077908-2077909
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10039392	0.88[ASN][1000 genomes]
rs10039393	0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs10062706	0.84[ASN][1000 genomes]
rs10066597	0.88[ASN][1000 genomes]
rs10067919	0.88[ASN][1000 genomes]
rs10068634	0.88[ASN][1000 genomes]
rs10076573	0.81[ASN][1000 genomes]
rs11133925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12054704	0.96[ASN][1000 genomes]
rs12054740	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4246755	0.91[ASN][1000 genomes]
rs4299769	0.80[ASN][1000 genomes]
rs4361563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4568402	0.81[ASN][1000 genomes]
rs55637118	0.88[ASN][1000 genomes]
rs55637204	0.88[ASN][1000 genomes]
rs55719457	0.88[ASN][1000 genomes]
rs55791921	0.88[ASN][1000 genomes]
rs55920103	0.88[ASN][1000 genomes]
rs56125143	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56130408	0.88[ASN][1000 genomes]
rs56173153	0.88[ASN][1000 genomes]
rs56186338	0.88[ASN][1000 genomes]
rs56188011	0.88[ASN][1000 genomes]
rs56277896	0.88[ASN][1000 genomes]
rs56292928	0.81[ASN][1000 genomes]
rs56365450	0.88[ASN][1000 genomes]
rs56408053	0.83[ASN][1000 genomes]
rs58739107	0.88[ASN][1000 genomes]
rs59104705	0.88[ASN][1000 genomes]
rs59337987	0.88[ASN][1000 genomes]
rs59685893	0.88[ASN][1000 genomes]
rs60006209	0.88[ASN][1000 genomes]
rs60697393	0.88[ASN][1000 genomes]
rs61623125	0.88[ASN][1000 genomes]
rs6869000	0.88[ASN][1000 genomes]
rs6869329	0.88[ASN][1000 genomes]
rs72708656	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72708663	0.94[ASN][1000 genomes]
rs72708679	0.88[ASN][1000 genomes]
rs72708681	0.88[ASN][1000 genomes]
rs72708682	0.86[ASN][1000 genomes]
rs72708684	0.88[ASN][1000 genomes]
rs72708689	0.88[ASN][1000 genomes]
rs72708693	0.88[ASN][1000 genomes]
rs72708694	0.88[ASN][1000 genomes]
rs72708697	0.88[ASN][1000 genomes]
rs72708698	0.88[ASN][1000 genomes]
rs72708699	0.88[ASN][1000 genomes]
rs72708702	0.88[ASN][1000 genomes]
rs72710605	0.81[ASN][1000 genomes]
rs7702195	0.95[JPT][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
3	nsv915846	chr5:1891098-2167677	Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1026930	chr5:1898993-2126061	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv427705	chr5:1950467-2115059	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1032759	chr5:2044117-2091631	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1020211	chr5:2045699-2104887	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv523478	chr5:2075162-2091155	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:2077800-2078600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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