Variant report

Variant	rs9493822
Chromosome Location	chr6:134398156-134398157
allele	A/G
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	chr6:134395600-134405000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:134395800-134398200	Weak transcription	HUVEC	blood vessel
3	chr6:134396000-134398800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:134396200-134399600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:134396200-134400800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:134396600-134401000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:134396800-134402800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:134397600-134399000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:134397600-134401800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:134397800-134398400	Enhancers	Placenta	Placenta

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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