Variant report

Variant	rs59723907
Chromosome Location	chr5:111481436-111481437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:111474504..111476934-chr5:111480612..111482796,2	K562	blood:
2	chr5:111480523..111483778-chr5:111495014..111499185,3	K562	blood:
3	chr5:111480653..111483715-chr5:111488508..111491421,3	K562	blood:

Variant related genes	Relation type
ENSG00000224032	Chromatin interaction
ENSG00000238363	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10515440	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17134157	0.85[AFR][1000 genomes]
rs30290	1.00[ASN][1000 genomes]
rs376888	0.94[ASN][1000 genomes]
rs56729311	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57764435	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59486872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6594563	0.82[ASN][1000 genomes]
rs73227477	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv599370	chr5:111419303-111485372	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	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:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111478800-111481600	Weak transcription	Fetal Muscle Leg	muscle
2	chr5:111478800-111481600	Weak transcription	NHDF-Ad	bronchial
3	chr5:111478800-111481800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr5:111479000-111481600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:111479000-111481800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr5:111479200-111481800	Weak transcription	NHEK	skin
7	chr5:111479400-111482000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:111479600-111481600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr5:111479600-111481600	Weak transcription	HMEC	breast
10	chr5:111479600-111481800	Weak transcription	Fetal Stomach	stomach
11	chr5:111479600-111481800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr5:111479600-111482000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:111481200-111481600	Enhancers	GM12878-XiMat	blood
14	chr5:111481200-111482800	Enhancers	Adipose Nuclei	Adipose
15	chr5:111481200-111482800	Enhancers	Fetal Lung	lung
16	chr5:111481200-111483200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:111481400-111482400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:111481400-111482800	Enhancers	Muscle Satellite Cultured Cells	--
19	chr5:111481400-111482800	Enhancers	Fetal Heart	heart
20	chr5:111481400-111482800	Enhancers	NHLF	lung
21	chr5:111481400-111482800	Enhancers	Osteobl	bone

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