Variant report

Variant	rs56386819
Chromosome Location	chr2:181889189-181889190
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	chr2:181856800-181897200	Weak transcription	Primary B cells from cord blood	blood
2	chr2:181857800-181901200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:181860000-181894800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr2:181873400-181901000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:181873600-181889600	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:181885000-181890600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:181885800-181889600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:181886000-181901200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:181887800-181889200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:181887800-181889800	Weak transcription	Fetal Heart	heart
11	chr2:181887800-181890800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:181888200-181891000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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