Variant report

Variant	rs569666099
Chromosome Location	chr8:64514038-64514039
allele	A/G
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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv1529617	chr8:64514036-64514039	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64505000-64514400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:64509800-64516000	Weak transcription	Brain Germinal Matrix	brain
3	chr8:64510200-64515000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:64513000-64514800	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr8:64513600-64515600	Weak transcription	Fetal Brain Male	brain

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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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