Variant report

Variant	rs117853228
Chromosome Location	chr6:71861804-71861805
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	esv17967	chr6:71860706-71862638	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71856400-71863600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:71861600-71862000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:71861600-71862000	Enhancers	Brain Anterior Caudate	brain
4	chr6:71861800-71862000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:71861800-71862000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:71861800-71862000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:71861800-71862000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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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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