Variant report

Variant	rs146750165
Chromosome Location	chr6:133893132-133893133
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886682	chr6:133892208-133943732	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133891200-133895200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:133891200-133895200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:133891200-133895200	Weak transcription	NHDF-Ad	bronchial
4	chr6:133891200-133895200	Weak transcription	Osteobl	bone
5	chr6:133891200-133895400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:133891400-133895200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:133891600-133895200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:133891800-133893200	Enhancers	Fetal Lung	lung
9	chr6:133892200-133895400	Weak transcription	A549	lung
10	chr6:133893000-133893200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:133893000-133893400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:133893000-133893600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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