Variant report

Variant	rs62251131
Chromosome Location	chr3:28398703-28398704
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	chr3:28388460..28394013-chr3:28397646..28403545,9	K562	blood:

Variant related genes	Relation type
ENSG00000163512	Chromatin interaction
ENSG00000206559	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1037723	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11705962	0.87[ASN][1000 genomes]
rs11706332	0.89[ASN][1000 genomes]
rs11707705	0.93[ASN][1000 genomes]
rs11710963	0.95[ASN][1000 genomes]
rs11712484	0.88[ASN][1000 genomes]
rs11712489	0.88[ASN][1000 genomes]
rs11720107	0.93[ASN][1000 genomes]
rs11918050	0.96[ASN][1000 genomes]
rs11921692	0.96[ASN][1000 genomes]
rs11924173	0.96[ASN][1000 genomes]
rs11926399	0.93[ASN][1000 genomes]
rs13066118	0.85[ASN][1000 genomes]
rs13069839	0.81[ASN][1000 genomes]
rs13074633	0.93[ASN][1000 genomes]
rs13075840	0.93[ASN][1000 genomes]
rs13080155	0.93[ASN][1000 genomes]
rs13081520	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13081787	0.91[ASN][1000 genomes]
rs13087143	0.93[ASN][1000 genomes]
rs13087774	0.93[ASN][1000 genomes]
rs13088574	0.93[ASN][1000 genomes]
rs13090439	0.96[ASN][1000 genomes]
rs13095628	0.96[ASN][1000 genomes]
rs13095675	0.82[ASN][1000 genomes]
rs13099152	0.86[ASN][1000 genomes]
rs1457909	0.88[ASN][1000 genomes]
rs1457910	0.93[ASN][1000 genomes]
rs1606386	0.87[ASN][1000 genomes]
rs1606388	0.82[ASN][1000 genomes]
rs17021402	0.96[ASN][1000 genomes]
rs17357206	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17638742	0.86[ASN][1000 genomes]
rs17638782	0.86[ASN][1000 genomes]
rs17638991	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17695765	0.88[ASN][1000 genomes]
rs17695884	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696025	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17696459	0.93[ASN][1000 genomes]
rs17696561	0.93[ASN][1000 genomes]
rs17696783	0.91[ASN][1000 genomes]
rs1975828	0.82[ASN][1000 genomes]
rs1975829	0.80[ASN][1000 genomes]
rs34311197	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34574968	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34796684	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35088087	0.96[ASN][1000 genomes]
rs35137555	0.88[ASN][1000 genomes]
rs35177150	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35702956	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35736614	0.86[ASN][1000 genomes]
rs35825908	0.91[ASN][1000 genomes]
rs35845822	0.86[ASN][1000 genomes]
rs36051688	0.96[ASN][1000 genomes]
rs36105900	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3762797	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4234337	0.86[ASN][1000 genomes]
rs4256085	0.86[ASN][1000 genomes]
rs4295137	0.86[ASN][1000 genomes]
rs4322963	0.86[ASN][1000 genomes]
rs4428136	0.84[ASN][1000 genomes]
rs4450765	0.86[ASN][1000 genomes]
rs4452283	0.96[ASN][1000 genomes]
rs4522735	0.86[ASN][1000 genomes]
rs4680750	0.82[ASN][1000 genomes]
rs4680753	0.86[ASN][1000 genomes]
rs58918848	0.96[ASN][1000 genomes]
rs59975750	0.95[ASN][1000 genomes]
rs60043893	0.95[ASN][1000 genomes]
rs62250271	0.93[ASN][1000 genomes]
rs62250272	0.93[ASN][1000 genomes]
rs62250273	0.92[ASN][1000 genomes]
rs62250296	0.91[ASN][1000 genomes]
rs62251105	0.88[ASN][1000 genomes]
rs62251108	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62251134	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62251138	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62251144	0.93[ASN][1000 genomes]
rs62252069	0.86[ASN][1000 genomes]
rs6551255	0.96[ASN][1000 genomes]
rs66733194	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66767946	0.87[ASN][1000 genomes]
rs6763313	0.82[ASN][1000 genomes]
rs6771057	0.82[ASN][1000 genomes]
rs6771460	0.96[ASN][1000 genomes]
rs68085718	0.96[ASN][1000 genomes]
rs71087683	0.86[ASN][1000 genomes]
rs7434193	0.96[ASN][1000 genomes]
rs7627471	0.85[ASN][1000 genomes]
rs7627575	0.86[ASN][1000 genomes]
rs7635383	0.87[ASN][1000 genomes]
rs7638450	0.93[ASN][1000 genomes]
rs7639750	0.82[ASN][1000 genomes]
rs7643191	0.88[ASN][1000 genomes]
rs7649498	0.82[ASN][1000 genomes]
rs7650831	0.84[ASN][1000 genomes]
rs952888	0.86[ASN][1000 genomes]
rs9683360	0.91[ASN][1000 genomes]
rs969443	0.91[ASN][1000 genomes]
rs9843464	0.82[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	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28393800-28412200	Weak transcription	Pancreas	Pancrea
2	chr3:28398600-28399000	ZNF genes & repeats	Brain Germinal Matrix	brain

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