Variant report

Variant	rs117549743
Chromosome Location	chr11:106595834-106595835
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898359	chr11:106523574-106656863	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv898360	chr11:106566114-106598286	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv898361	chr11:106567910-106598286	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2590906	chr11:106595357-106596735	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
5	esv2222990	chr11:106595688-106596355	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3466175	chr11:106595745-106596272	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3500449	chr11:106595760-106596283	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3500450	chr11:106595768-106596269	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv9628	chr11:106595782-106596295	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3500446	chr11:106595789-106596201	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3466130	chr11:106595801-106596238	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3500448	chr11:106595812-106596217	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3466152	chr11:106595817-106596192	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3466163	chr11:106595820-106596238	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3402746	chr11:106595832-106596187	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106552800-106628200	Weak transcription	Pancreas	Pancrea
2	chr11:106583600-106598000	Weak transcription	Fetal Brain Male	brain
3	chr11:106595600-106604800	Weak transcription	Fetal Lung	lung
4	chr11:106595800-106603400	Weak transcription	Adipose Derived Mesenchymal Stem Cell 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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