Variant report

Variant rs7594895
Chromosome Location chr2:180436657-180436658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180433000-180440800 Weak transcription Gastric stomach
2 chr2:180433000-180445600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr2:180434000-180438600 Enhancers HepG2 liver
4 chr2:180434200-180437600 Enhancers Skeletal Muscle Male skeletal muscle
5 chr2:180435000-180438600 Weak transcription Osteobl bone
6 chr2:180435000-180438800 Weak transcription Fetal Lung lung
7 chr2:180435200-180461000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:180435400-180438600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr2:180435400-180446400 Weak transcription Fetal Kidney kidney
10 chr2:180435800-180438400 Enhancers Liver Liver
11 chr2:180436200-180439000 Weak transcription Fetal Intestine Large intestine
12 chr2:180436400-180436800 Enhancers Psoas Muscle Psoas
13 chr2:180436400-180437000 Weak transcription Skeletal Muscle Female skeletal muscle
14 chr2:180436600-180436800 ZNF genes & repeats Fetal Intestine Small intestine
15 chr2:180436600-180437000 Enhancers Lung lung

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