Variant report

Variant rs73088321
Chromosome Location chr5:35483574-35483575
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:35479800-35488600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr5:35480200-35483800 Weak transcription Colon Smooth Muscle Colon
3 chr5:35481600-35483800 Enhancers HepG2 liver
4 chr5:35481600-35485200 Enhancers Primary monocytes fromperipheralblood blood
5 chr5:35482000-35485000 Enhancers Primary neutrophils fromperipheralblood blood
6 chr5:35482000-35485200 Enhancers Fetal Kidney kidney
7 chr5:35482200-35484800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr5:35482200-35485000 Enhancers Primary hematopoietic stem cells blood
9 chr5:35482400-35484600 Enhancers Fetal Lung lung
10 chr5:35482400-35485000 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr5:35482400-35485200 Enhancers Fetal Intestine Large intestine
12 chr5:35482400-35486200 Enhancers Liver Liver
13 chr5:35482600-35486200 Weak transcription iPS-15b Cell Line embryonic stem cell
14 chr5:35482800-35484800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr5:35482800-35485600 Weak transcription iPS-20b Cell Line embryonic stem cell
16 chr5:35482800-35486800 Weak transcription Esophagus oesophagus
17 chr5:35483000-35486800 Weak transcription Ovary ovary
18 chr5:35483200-35483600 Weak transcription Primary hematopoietic stem cells short term culture blood
19 chr5:35483200-35483800 Weak transcription Fetal Stomach stomach
20 chr5:35483200-35484400 Weak transcription Fetal Intestine Small intestine
21 chr5:35483200-35484600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
22 chr5:35483400-35483600 Enhancers HUES6 Cell Line embryonic stem cell
23 chr5:35483400-35483800 Enhancers Monocytes-CD14+_RO01746 blood
24 chr5:35483400-35484800 Weak transcription HUES48 Cell Line embryonic stem cell

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