Variant report

Variant	rs56938777
Chromosome Location	chr8:110150554-110150555
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110146800-110152400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:110147000-110152000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:110147000-110152400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr8:110150000-110151200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr8:110150000-110151400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr8:110150000-110151600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:110150000-110151800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:110150200-110151200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr8:110150200-110151400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:110150400-110151000	Enhancers	HUES6 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