Variant report

Variant	rs1028196
Chromosome Location	chr4:124976426-124976427
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1519232	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2176663	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57599742	1.00[EUR][1000 genomes]
rs57715760	1.00[EUR][1000 genomes]
rs58940197	1.00[EUR][1000 genomes]
rs60728469	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv868977	chr4:124841128-125550637	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1014750	chr4:124966525-125111807	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1000839	chr4:124966525-125115590	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124974600-124976800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:124975200-124981600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:124975400-124976600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:124975600-124977200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr4:124975600-124977600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:124975600-124981000	Weak transcription	HUVEC	blood vessel
7	chr4:124976000-124976800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:124976000-124977800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:124976200-124976800	Enhancers	NHLF	lung
10	chr4:124976400-124976800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:124976400-124976800	Enhancers	Aorta	Aorta
12	chr4:124976400-124977400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:124976400-124977400	Enhancers	Osteobl	bone
14	chr4:124976400-124977800	Enhancers	HUES6 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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