Variant report

Variant rs1546603
Chromosome Location chr2:180435707-180435708
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180427400-180436400 Weak transcription Psoas Muscle Psoas
2 chr2:180433000-180440800 Weak transcription Gastric stomach
3 chr2:180433000-180445600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:180433800-180436400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr2:180434000-180438600 Enhancers HepG2 liver
6 chr2:180434200-180436200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr2:180434200-180437600 Enhancers Skeletal Muscle Male skeletal muscle
8 chr2:180434400-180436000 Enhancers NHDF-Ad bronchial
9 chr2:180435000-180436600 Weak transcription Fetal Intestine Small intestine
10 chr2:180435000-180438600 Weak transcription Osteobl bone
11 chr2:180435000-180438800 Weak transcription Fetal Lung lung
12 chr2:180435200-180461000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:180435400-180436200 Weak transcription Skeletal Muscle Female skeletal muscle
14 chr2:180435400-180438600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr2:180435400-180446400 Weak transcription Fetal Kidney kidney
16 chr2:180435600-180436000 Weak transcription Fetal Intestine Large intestine

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