Variant report

Variant rs1938562
Chromosome Location chr1:98473716-98473717
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:98463800-98499800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:98465200-98474000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr1:98466400-98475600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr1:98468200-98474000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr1:98470400-98476600 Enhancers Osteobl bone
6 chr1:98471600-98486600 Weak transcription HSMM muscle
7 chr1:98471800-98474000 Weak transcription NHDF-Ad bronchial
8 chr1:98472400-98473800 Enhancers A549 lung
9 chr1:98472600-98476000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:98472800-98475600 Enhancers HUVEC blood vessel
11 chr1:98473000-98474000 Weak transcription NHLF lung
12 chr1:98473400-98473800 Weak transcription Muscle Satellite Cultured Cells --
13 chr1:98473400-98474800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr1:98473600-98474200 Enhancers Primary T killer naive cells fromperipheralblood blood

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