Variant report

Variant	rs2370737
Chromosome Location	chr2:187881494-187881495
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:187867683..187871574-chr2:187879806..187883521,7	K562	blood:
2	chr2:187873118..187875101-chr2:187880377..187882881,2	K562	blood:
3	chr2:187867081..187871574-chr2:187878327..187884066,8	K562	blood:
4	chr2:187880614..187882392-chr2:187883070..187885424,2	K562	blood:

Variant related genes	Relation type
ENSG00000226553	Chromatin interaction
ENSG00000224063	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10931267	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11894779	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12465733	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12469871	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12471570	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12616398	0.81[AMR][1000 genomes]
rs13000137	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13005588	0.83[AMR][1000 genomes]
rs13024632	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs13431778	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16828625	0.81[ASN][1000 genomes]
rs2370734	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2370735	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2887838	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34460383	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs34938912	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35252928	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3845713	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3856420	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4093127	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4277485	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4667133	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56121767	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6733991	0.81[ASN][1000 genomes]
rs72904956	0.81[AMR][1000 genomes]
rs72910639	0.83[AMR][1000 genomes]
rs7602307	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7602536	0.90[ASN][1000 genomes]
rs7602852	0.85[EUR][1000 genomes];0.92[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	nsv949700	chr2:187713412-188361211	Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv528437	chr2:187778830-187907901	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv999207	chr2:187787121-187924667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv536084	chr2:187787121-187924667	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv875553	chr2:187856937-188067355	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv875554	chr2:187873808-187964942	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv834486	chr2:187876328-188032965	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 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	chr2:187875800-187885200	Weak transcription	Psoas Muscle	Psoas

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