Variant report

Variant	rs571404745
Chromosome Location	chr6:75733115-75733116
allele	C/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	nsv830696	chr6:75538316-75734609	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv970729	chr6:75731546-75735559	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75730800-75734600	Weak transcription	Fetal Lung	lung
2	chr6:75731600-75733200	Weak transcription	Osteobl	bone
3	chr6:75732200-75734000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:75733000-75733200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:75733000-75733600	Enhancers	Fetal Kidney	kidney
6	chr6:75733000-75733800	Enhancers	NHDF-Ad	bronchial
7	chr6:75733000-75733800	Enhancers	NHLF	lung
8	chr6:75733000-75735600	Enhancers	HUVEC	blood vessel

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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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