Variant report

Variant	rs59882748
Chromosome Location	chr1:47673503-47673504
allele	A/G
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	chr1:47659000-47675800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:47664600-47676000	Weak transcription	K562	blood
3	chr1:47671400-47674600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:47671600-47673800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:47672800-47673600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:47673200-47674200	Enhancers	HUVEC	blood vessel
7	chr1:47673200-47674800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:47673400-47674000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr1:47673400-47674200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:47673400-47674800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:47673400-47675600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:47673400-47677600	Enhancers	HMEC	breast

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

what's new

Quick links