Variant report

Variant	rs73724928
Chromosome Location	chr6:15930169-15930170
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15926000-15931000	Weak transcription	Aorta	Aorta
2	chr6:15927600-15930200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr6:15928000-15936400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:15928600-15930800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr6:15928800-15930200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr6:15929400-15930600	Enhancers	Adipose Nuclei	Adipose
7	chr6:15930000-15930800	Weak transcription	Placenta	Placenta
8	chr6:15930000-15930800	Enhancers	Monocytes-CD14+_RO01746	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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