Variant report

Variant	rs531063760
Chromosome Location	chr15:60159634-60159635
allele	C/G
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	nsv904280	chr15:60042722-60524025	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv275017	chr15:60155312-60159639	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60159000-60159800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr15:60159200-60159800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:60159200-60159800	Enhancers	Fetal Brain Male	brain
4	chr15:60159400-60159800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:60159400-60159800	Enhancers	Fetal Brain Female	brain
6	chr15:60159600-60159800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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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