Variant report

Variant rs60549042
Chromosome Location chr3:53650148-53650149
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:53635400-53650200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr3:53639400-53650200 Weak transcription Fetal Intestine Small intestine
3 chr3:53640000-53650800 Weak transcription Fetal Intestine Large intestine
4 chr3:53645400-53651000 Weak transcription Lung lung
5 chr3:53646800-53651000 Weak transcription Spleen Spleen
6 chr3:53647000-53650200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr3:53647000-53650400 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr3:53648800-53651600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr3:53649400-53650200 Weak transcription Primary B cells from peripheral blood blood
10 chr3:53649600-53651200 Enhancers Primary monocytes fromperipheralblood blood
11 chr3:53649800-53650800 Weak transcription Colonic Mucosa Colon
12 chr3:53650000-53650400 Enhancers Fetal Brain Male brain
13 chr3:53650000-53651000 Bivalent Enhancer Adipose Nuclei Adipose
14 chr3:53650000-53651200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr3:53650000-53651200 Weak transcription Brain Hippocampus Middle brain
16 chr3:53650000-53651200 Enhancers Pancreatic Islets Pancreatic Islet
17 chr3:53650000-53651400 Enhancers Fetal Kidney kidney
18 chr3:53650000-53651400 Enhancers Monocytes-CD14+_RO01746 blood
19 chr3:53650000-53652000 Enhancers Fetal Lung lung

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