Variant report

Variant	rs4833918
Chromosome Location	chr4:124359609-124359610
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10026901	1.00[ASN][1000 genomes]
rs12330981	0.95[EUR][1000 genomes]
rs442351	0.80[AMR][1000 genomes]
rs4833916	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs623936	0.80[AMR][1000 genomes]
rs6852974	0.81[EUR][1000 genomes];1.00[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	nsv1006945	chr4:124206328-124503863	Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv537240	chr4:124206328-124503863	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv595379	chr4:124337522-124395024	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1014618	chr4:124350676-124391697	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv968799	chr4:124352929-124362179	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124355800-124365400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:124357800-124360000	Weak transcription	Lung	lung
3	chr4:124357800-124364000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:124357800-124365000	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr4:124359000-124359800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:124359000-124359800	Enhancers	Adipose Nuclei	Adipose
7	chr4:124359000-124359800	Enhancers	Fetal Lung	lung
8	chr4:124359000-124359800	Enhancers	Stomach Mucosa	stomach
9	chr4:124359200-124360000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:124359400-124359800	Enhancers	HepG2	liver
11	chr4:124359600-124364000	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr4:124359600-124364000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:124359600-124364600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:124359600-124364600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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