Variant report

Variant rs10191369
Chromosome Location chr2:180445997-180445998
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180435200-180461000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:180435400-180446400 Weak transcription Fetal Kidney kidney
3 chr2:180439800-180446400 Enhancers Liver Liver
4 chr2:180442400-180446800 Enhancers HepG2 liver
5 chr2:180445000-180446200 Enhancers Fetal Heart heart
6 chr2:180445200-180446000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr2:180445200-180450600 Enhancers Skeletal Muscle Male skeletal muscle
8 chr2:180445600-180449400 Weak transcription Right Atrium heart
9 chr2:180445800-180449200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr2:180445800-180449200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:180445800-180449200 Weak transcription Skeletal Muscle Female skeletal muscle

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