Variant report

Variant	rs182382222
Chromosome Location	chr2:49848328-49848329
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002841	chr2:49747904-49863227	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv535690	chr2:49747904-49863227	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv457563	chr2:49758675-49862134	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv581835	chr2:49758675-49862134	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv874026	chr2:49829630-49888676	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv430991	chr2:49836326-49971708	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:49847800-49848800	Enhancers	Fetal Heart	heart

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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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