Variant report

Variant	rs16937537
Chromosome Location	chr8:49419182-49419183
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49414200-49420000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:49414400-49419800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:49414600-49427000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr8:49415400-49422000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:49415600-49420400	Weak transcription	NHDF-Ad	bronchial
6	chr8:49415800-49425200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:49418800-49426200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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