Variant report

Variant	rs148864692
Chromosome Location	chr5:91863319-91863320
allele	A/T
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	nsv4915	chr5:91836073-91876327	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv969234	chr5:91862074-91866671	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91854600-91864200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr5:91862600-91864400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:91862800-91863800	Enhancers	HSMMtube	muscle
4	chr5:91862800-91863800	Enhancers	Osteobl	bone
5	chr5:91862800-91864400	Enhancers	NHDF-Ad	bronchial
6	chr5:91863000-91863400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
7	chr5:91863000-91863400	Enhancers	Ovary	ovary
8	chr5:91863000-91863600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr5:91863000-91864200	Enhancers	HSMM	muscle
10	chr5:91863000-91864400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links