Variant report

Variant	rs16939088
Chromosome Location	chr8:49843023-49843024
allele	C/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	chr8:49836800-49843200	Weak transcription	Esophagus	oesophagus
2	chr8:49837800-49846200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:49842000-49846400	Weak transcription	HMEC	breast
4	chr8:49842200-49846400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:49842800-49843400	Enhancers	GM12878-XiMat	blood
6	chr8:49843000-49843400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:49843000-49843400	Enhancers	NH-A	brain
8	chr8:49843000-49843400	Enhancers	Osteobl	bone

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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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