Variant report

Variant	rs80078817
Chromosome Location	chr11:33806454-33806455
allele	-/TTG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv975165	chr11:33806356-33809766	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
2	esv1238743	chr11:33806453-33806454	Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
3	nsv33970	chr11:33806455-33806455	Weak transcription	Chromatin interactive region	2 gene(s)	n/a	n/a
4	esv2373422	chr11:33806455-33806457	Weak transcription	Chromatin interactive region	2 gene(s)	n/a	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33802200-33818200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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