Variant report

Variant	rs56375234
Chromosome Location	chr2:30619745-30619746
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:30617933..30621462-chr2:30622789..30624514,3	K562	blood:
2	chr2:30618142..30620784-chr2:30680796..30682766,2	K562	blood:
3	chr2:30609954..30612791-chr2:30617529..30620270,2	K562	blood:
4	chr2:30618571..30622789-chr2:30622802..30626896,4	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10514771	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11127274	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11127275	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11885821	0.88[EUR][1000 genomes]
rs11885871	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11889918	0.87[EUR][1000 genomes]
rs12468604	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12471197	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12471227	0.92[EUR][1000 genomes]
rs12471481	0.91[EUR][1000 genomes]
rs12475327	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12988691	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12989601	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13017527	0.87[EUR][1000 genomes]
rs13029614	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13034878	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1357851	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34145247	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34600627	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35211324	0.80[EUR][1000 genomes]
rs4572642	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4613331	0.90[EUR][1000 genomes]
rs6706101	0.87[EUR][1000 genomes]
rs6710587	0.89[EUR][1000 genomes]
rs6712757	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6719566	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6723368	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6726574	0.89[EUR][1000 genomes]
rs6735708	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6748329	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6748436	0.87[EUR][1000 genomes]
rs6752411	0.86[EUR][1000 genomes]
rs7599885	0.80[EUR][1000 genomes]
rs894787	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[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	nsv533886	chr2:30130019-31068764	ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv833648	chr2:30505882-30696275	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv873769	chr2:30585638-30625264	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3459512	chr2:30615052-30627922	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3459513	chr2:30615052-30627922	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv11669	chr2:30615374-30627773	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2763638	chr2:30615651-30627654	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30617400-30621000	Weak transcription	Fetal Lung	lung
2	chr2:30618800-30621800	Enhancers	Ovary	ovary
3	chr2:30619000-30624800	Weak transcription	Fetal Heart	heart
4	chr2:30619400-30619800	Enhancers	Left Ventricle	heart
5	chr2:30619400-30619800	Enhancers	A549	lung
6	chr2:30619400-30620000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:30619400-30621200	Enhancers	Pancreas	Pancrea
8	chr2:30619400-30637200	Enhancers	Fetal Stomach	stomach
9	chr2:30619600-30623600	Weak transcription	Right Ventricle	heart

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