Variant report

Variant	rs73771464
Chromosome Location	chr6:126701006-126701007
allele	C/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	chr6:126665400-126702200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:126665400-126702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:126678800-126702400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:126694000-126708800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:126694600-126701800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:126699000-126701800	Enhancers	Colon Smooth Muscle	Colon
7	chr6:126700000-126701200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:126700400-126702400	Enhancers	Liver	Liver
9	chr6:126700600-126701200	Enhancers	HepG2	liver
10	chr6:126701000-126702200	Weak transcription	ES-UCSF4 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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