Variant report

Variant	rs11117732
Chromosome Location	chr1:217120054-217120055
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217111000-217125400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:217117800-217120800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr1:217117800-217121200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:217118400-217120200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr1:217118800-217125400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr1:217119400-217120800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:217119600-217125400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:217119600-217125400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:217119800-217120200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr1:217119800-217120800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:217119800-217121000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:217119800-217126000	Weak transcription	iPS-18 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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