Variant report

Variant	rs188294011
Chromosome Location	chr1:56623677-56623678
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	esv3436415	chr1:56623664-56625062	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56619400-56624800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:56621400-56624000	Enhancers	Dnd41	blood
3	chr1:56622400-56624000	Enhancers	Fetal Thymus	thymus
4	chr1:56622600-56623800	Enhancers	Thymus	Thymus
5	chr1:56622600-56624000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:56622600-56624000	Enhancers	Primary T cells from cord blood	blood
7	chr1:56623400-56624600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr1:56623600-56626400	Weak transcription	Fetal Kidney	kidney

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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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