Variant report

Variant	rs180870252
Chromosome Location	chr6:71662408-71662409
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	nsv886148	chr6:71623253-71694742	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71662000-71662800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr6:71662200-71662600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
3	chr6:71662200-71662600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:71662200-71662600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:71662200-71662800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr6:71662200-71663400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr6:71662400-71662600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:71662400-71662600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr6:71662400-71662800	Flanking Active TSS	Fetal Brain Female	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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