Variant report

Variant	rs56037558
Chromosome Location	chr2:11847880-11847881
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:11845672..11848485-chr2:11854738..11857350,2	K562	blood:
2	chr2:11846985..11850367-chr2:11854727..11856903,3	K562	blood:
3	chr2:11846487..11849163-chr2:11861394..11864820,3	K562	blood:

Variant related genes	Relation type
ENSG00000134324	Chromatin interaction
ENSG00000203643	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs56122279	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56266446	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56958924	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57097271	0.93[AFR][1000 genomes]
rs57245099	0.82[AFR][1000 genomes]
rs58429439	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59002621	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61153226	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61602903	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915489	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915494	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915497	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915498	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73915500	1.00[AMR][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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats 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 miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
4	nsv469449	chr2:11808654-11854012	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv580972	chr2:11808654-11854012	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr2:11837800-11848200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:11838600-11848000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:11841600-11850000	Weak transcription	Brain Substantia Nigra	brain
4	chr2:11841600-11850000	Weak transcription	Ovary	ovary
5	chr2:11841600-11850200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr2:11841800-11850200	Weak transcription	Brain Angular Gyrus	brain
7	chr2:11844200-11854200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr2:11844600-11849800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:11844600-11849800	Weak transcription	NH-A	brain
10	chr2:11844600-11849800	Weak transcription	NHLF	lung
11	chr2:11844600-11856400	Weak transcription	Psoas Muscle	Psoas
12	chr2:11844800-11850000	Weak transcription	NHDF-Ad	bronchial
13	chr2:11845000-11848200	Weak transcription	Osteobl	bone
14	chr2:11845000-11849800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:11845800-11848000	Weak transcription	Pancreas	Pancrea
16	chr2:11845800-11851000	Weak transcription	Liver	Liver
17	chr2:11847400-11848000	Enhancers	Fetal Lung	lung
18	chr2:11847600-11848800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr2:11847800-11848600	Enhancers	Placenta	Placenta
20	chr2:11847800-11850000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:11847800-11850200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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