Variant report

Variant	rs73780425
Chromosome Location	chr6:143847323-143847324
allele	A/G
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	chr6:143833200-143849600	Weak transcription	Primary T cells from cord blood	blood
2	chr6:143833400-143849400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:143834600-143855800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr6:143835000-143850000	Weak transcription	Fetal Intestine Large	intestine
5	chr6:143836800-143848400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr6:143843800-143847800	Weak transcription	Aorta	Aorta
7	chr6:143845400-143847400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:143845400-143847400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr6:143846800-143847400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:143846800-143849400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:143847000-143849000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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