Variant report

Variant	rs565222292
Chromosome Location	chr1:85204398-85204399
allele	C/G
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	esv3413749	chr1:85203614-85205762	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	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	chr1:85203800-85204400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:85204000-85204400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:85204200-85205000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr1:85204200-85205400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr1:85204200-85212800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:85204200-85230400	Weak transcription	iPS DF 6.9 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

what's new

Quick links