Variant report

Variant	rs530662680
Chromosome Location	chr2:172998217-172998218
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	esv1827284	chr2:172997770-173006567	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172995800-172999400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr2:172996400-172998400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:172996800-172998400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:172997200-172998400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:172997400-172998800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:172997800-172998400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr2:172998000-172999200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr2:172998200-172999200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

Quick Search:

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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