Variant report

Variant	rs72715725
Chromosome Location	chr14:55733965-55733966
allele	C/T
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]
rs72715735	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][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	esv3396352	chr14:55731649-55734247	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55730600-55735000	Weak transcription	HSMMtube	muscle
2	chr14:55730600-55737400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:55732600-55737400	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr14:55733000-55735400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr14:55733400-55734200	Weak transcription	Fetal Lung	lung
6	chr14:55733400-55735200	Enhancers	Fetal Heart	heart
7	chr14:55733800-55734000	Enhancers	Lung	lung

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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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