Variant report

Variant	rs72953127
Chromosome Location	chr3:70567919-70567920
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs13434066	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	nsv999046	chr3:70549472-70576944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70565400-70568400	Enhancers	Fetal Muscle Leg	muscle
2	chr3:70566800-70568400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:70567600-70568400	Enhancers	Adipose Nuclei	Adipose
4	chr3:70567600-70568400	Enhancers	Aorta	Aorta
5	chr3:70567600-70570200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr3:70567800-70568000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr3:70567800-70568400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:70567800-70569200	Weak transcription	Fetal Lung	lung

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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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