Variant report

Variant rs1873347
Chromosome Location chr12:72980230-72980231
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:72958200-72984400 Weak transcription Pancreas Pancrea
2 chr12:72964400-72986800 Weak transcription Fetal Intestine Large intestine
3 chr12:72970600-72982800 Weak transcription Ovary ovary
4 chr12:72978800-72982000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:72979200-72980800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr12:72979200-72981000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr12:72979200-72981200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr12:72979800-72980800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr12:72980000-72980400 Enhancers HUES64 Cell Line embryonic stem cell
10 chr12:72980000-72980600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr12:72980000-72980600 Enhancers HUES6 Cell Line embryonic stem cell
12 chr12:72980200-72980600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr12:72980200-72980800 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr12:72980200-72980800 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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