Variant report

Variant	rs16866740
Chromosome Location	chr2:180330061-180330062
allele	C/T
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	chr2:180308200-180332600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180309200-180352200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr2:180325200-180351400	Weak transcription	Psoas Muscle	Psoas
4	chr2:180326200-180331800	Weak transcription	Osteobl	bone
5	chr2:180326800-180331800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:180327400-180331400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:180329400-180330200	Strong transcription	Liver	Liver
8	chr2:180329800-180331000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	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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