Variant report

Variant	rs2960663
Chromosome Location	chr10:117577223-117577224
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117576800-117577400	Enhancers	Fetal Intestine Small	intestine
2	chr10:117577000-117577400	Enhancers	Ovary	ovary
3	chr10:117577000-117577600	Enhancers	NHDF-Ad	bronchial
4	chr10:117577000-117577800	Enhancers	HSMM	muscle
5	chr10:117577200-117577400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:117577200-117577400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr10:117577200-117577400	Flanking Active TSS	Liver	Liver
8	chr10:117577200-117577400	Enhancers	Osteobl	bone
9	chr10:117577200-117577800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:117577200-117577800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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