Variant report

Variant	rs645201
Chromosome Location	chr6:147824674-147824675
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147821000-147827800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:147824200-147825400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
3	chr6:147824400-147824800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
4	chr6:147824400-147825200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
5	chr6:147824400-147825400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr6:147824400-147825400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr6:147824400-147825600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr6:147824600-147824800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
9	chr6:147824600-147824800	Flanking Bivalent TSS/Enh	iPS-20b 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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