Variant report

Variant	rs1852499
Chromosome Location	chr2:178880755-178880756
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:178875126..178877960-chr2:178878774..178881876,3	K562	blood:
2	chr2:178873991..178877960-chr2:178878774..178881876,4	K562	blood:

Variant related genes	Relation type
ENSG00000236664	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1020010	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs10211367	0.83[ASN][1000 genomes]
rs10930820	0.89[ASN][1000 genomes]
rs12473461	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12478277	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12478848	0.81[ASN][1000 genomes]
rs12618606	0.82[ASN][1000 genomes]
rs12621562	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs13030747	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1527286	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1527287	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1527293	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1534289	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1546813	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1554776	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17687590	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs17687668	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1821629	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1836672	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1852496	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1852497	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1982131	0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1991994	0.89[ASN][1000 genomes]
rs2060490	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2060491	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2117738	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2117740	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4335982	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4567975	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4893994	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4893995	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62183413	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6750869	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6758442	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs744397	0.83[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs744398	0.87[ASN][1000 genomes]
rs7570423	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs764780	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs934568	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9679090	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875451	chr2:178748294-178953409	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv998304	chr2:178756380-178924378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536056	chr2:178756380-178924378	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr2:178873600-178882800	Weak transcription	Pancreas	Pancrea
2	chr2:178873600-178889600	Weak transcription	A549	lung

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