Variant report

Variant	rs2836549
Chromosome Location	chr21:39968139-39968140
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39955800-39971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:39964400-39968800	Weak transcription	Spleen	Spleen
3	chr21:39965200-39969800	Weak transcription	Aorta	Aorta
4	chr21:39965400-39969400	Weak transcription	Fetal Brain Male	brain
5	chr21:39966600-39968400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr21:39966800-39968200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr21:39966800-39968200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr21:39966800-39968600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr21:39966800-39968600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr21:39967000-39968200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr21:39967000-39968400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr21:39967000-39971400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr21:39967200-39968400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr21:39967400-39968600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr21:39968000-39968600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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