Variant report

Variant	rs77962986
Chromosome Location	chr11:60084526-60084527
allele	-/CAGA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3449168	chr11:60084417-60085198	Weak transcription Flanking Active TSS Enhancers	lncRNA	1 gene(s)	inside rSNPs	n/a
2	esv2497712	chr11:60084526-60084529	Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
3	esv2034556	chr11:60084526-60084530	Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:60083800-60084600	Flanking Active TSS	GM12878-XiMat	blood
2	chr11:60083800-60086200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:60084400-60086400	Weak transcription	Placenta	Placenta

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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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