Variant report

Variant	rs199731731
Chromosome Location	chr5:91625097-91625098
allele	A/C
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	esv2646220	chr5:91625094-91625097	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	inside rSNPs	n/a
2	esv2127093	chr5:91625094-91625098	Active TSS Flanking Active TSS Enhancers	lncRNA	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	chr5:91624800-91625200	Enhancers	Left Ventricle	heart
2	chr5:91625000-91625200	Flanking Active TSS	Fetal Heart	heart
3	chr5:91625000-91626000	Active TSS	Right Atrium	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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