Variant report

Variant	rs10228780
Chromosome Location	chr7:147853080-147853081
allele	C/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	chr7:147850200-147853800	Enhancers	Fetal Heart	heart
2	chr7:147851200-147854200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:147851800-147854200	Enhancers	Ovary	ovary
4	chr7:147852400-147854200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:147852600-147853200	Enhancers	NH-A	brain
6	chr7:147852600-147854000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:147852800-147853200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:147852800-147853400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:147853000-147853200	Enhancers	Spleen	Spleen
10	chr7:147853000-147853400	Enhancers	Osteobl	bone
11	chr7:147853000-147853600	Enhancers	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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