Variant report

Variant	rs72925376
Chromosome Location	chr4:128077905-128077906
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs58127671	1.00[AMR][1000 genomes]
rs58944195	1.00[AMR][1000 genomes]
rs60943407	1.00[AMR][1000 genomes]
rs72925318	1.00[AMR][1000 genomes]
rs72925319	1.00[AMR][1000 genomes]
rs72925320	1.00[AMR][1000 genomes]
rs72925322	1.00[AMR][1000 genomes]
rs72925325	1.00[AMR][1000 genomes]
rs72925343	1.00[AMR][1000 genomes]
rs72925354	1.00[AMR][1000 genomes]
rs72925360	1.00[AMR][1000 genomes]
rs72925362	1.00[AMR][1000 genomes]
rs72925366	1.00[AMR][1000 genomes]
rs72925368	1.00[AMR][1000 genomes]
rs72925375	1.00[AMR][1000 genomes]
rs72925383	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879914	chr4:128005362-128123638	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128075400-128078800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:128077200-128078000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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