Variant report

Variant	rs62337588
Chromosome Location	chr4:160347937-160347938
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160339200-160348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:160345600-160348400	Weak transcription	HepG2	liver
3	chr4:160347000-160348200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr4:160347400-160348200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:160347400-160348600	Enhancers	H9 Cell Line	embryonic stem cell
6	chr4:160347400-160349400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:160347600-160348600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:160347600-160349200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:160347600-160351000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:160347600-160356800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:160347800-160350200	Weak transcription	HUES64 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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