Variant report

Variant	rs10072877
Chromosome Location	chr5:111858920-111858921
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs163454	0.86[EUR][1000 genomes]
rs163455	0.86[EUR][1000 genomes]
rs255704	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs255705	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs255707	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs338841	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs338848	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs338851	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs338852	0.93[ASN][1000 genomes]
rs338853	0.93[ASN][1000 genomes]
rs413345	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs442470	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv882715	chr5:111836278-111894491	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
3	nsv882716	chr5:111848890-111894491	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111855600-111859400	Enhancers	Primary B cells from cord blood	blood
2	chr5:111857800-111859200	Enhancers	Primary B cells from peripheral blood	blood
3	chr5:111858000-111860600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr5:111858400-111859400	Flanking Active TSS	GM12878-XiMat	blood
5	chr5:111858400-111860600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr5:111858600-111859200	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr5:111858600-111859400	Enhancers	Stomach Mucosa	stomach
8	chr5:111858600-111859600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:111858600-111859800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr5:111858600-111859800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr5:111858600-111860200	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr5:111858600-111860600	Enhancers	Adipose Nuclei	Adipose
13	chr5:111858800-111859200	Enhancers	H1 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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