Variant report

Variant	rs10483167
Chromosome Location	chr22:33325803-33325804
allele	G/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	chr22:33314000-33380800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr22:33314200-33332200	Weak transcription	HepG2	liver
3	chr22:33315600-33328200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr22:33319200-33333000	Weak transcription	Fetal Brain Male	brain
5	chr22:33319600-33326800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr22:33323800-33327600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
7	chr22:33324400-33327600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr22:33324800-33327600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr22:33325400-33328800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr22:33325400-33329200	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr22:33325400-33329400	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr22:33325600-33326600	Strong transcription	HUES6 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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