Variant report

Variant	rs72042807
Chromosome Location	chr19:51660896-51660897
allele	-/ACTTCCCAT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2535637	chr19:51660895-51660903	Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
2	esv2305697	chr19:51660895-51660904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51650400-51677000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:51654400-51661200	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr19:51658800-51661400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr19:51659800-51661400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr19:51660600-51666200	Weak transcription	GM12878-XiMat	blood
6	chr19:51660800-51661000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
7	chr19:51660800-51661400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr19:51660800-51661400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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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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