Variant report

Variant	rs2900060
Chromosome Location	chr5:111487149-111487150
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	chr5:111485629..111487985-chr5:111496588..111499466,2	K562	blood:

Variant related genes	Relation type
ENSG00000238363	Chromatin interaction
ENSG00000224032	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs17134155	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17265886	0.93[EUR][1000 genomes]
rs2290990	0.91[EUR][1000 genomes]
rs27982	0.82[ASN][1000 genomes]
rs55812441	0.86[EUR][1000 genomes]
rs56158171	0.93[EUR][1000 genomes]
rs57541807	1.00[ASN][1000 genomes]
rs60370278	1.00[ASN][1000 genomes]
rs61482608	0.93[EUR][1000 genomes]
rs6898536	1.00[ASN][1000 genomes]
rs73227487	0.82[ASN][1000 genomes]
rs73227490	1.00[ASN][1000 genomes]
rs73227492	1.00[ASN][1000 genomes]
rs73227493	1.00[ASN][1000 genomes]
rs73227496	1.00[ASN][1000 genomes]
rs73227498	1.00[ASN][1000 genomes]
rs73787775	1.00[ASN][1000 genomes]
rs73787781	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7449256	0.93[EUR][1000 genomes]
rs7700705	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7711555	0.93[EUR][1000 genomes]
rs7713216	0.90[EUR][1000 genomes]
rs7720064	0.93[EUR][1000 genomes]
rs7720344	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7730625	0.98[EUR][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	nsv599367	chr5:110924280-111602713	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1015302	chr5:111339022-111802947	Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv537861	chr5:111339022-111802947	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv948869	chr5:111476404-111695183	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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