Variant report

Variant	rs112683857
Chromosome Location	chr11:33994098-33994099
allele	A/C
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	esv3511616	chr11:33993774-33994639	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3511617	chr11:33993774-33994639	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3410723	chr11:33993778-33994481	Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33993000-33998200	Weak transcription	Hela-S3	cervix
2	chr11:33993200-33997800	Weak transcription	Adipose Nuclei	Adipose
3	chr11:33993200-33998000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr11:33993200-33998000	Weak transcription	Fetal Lung	lung
5	chr11:33994000-33994200	Flanking Active TSS	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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