Variant report

Variant rs2784058
Chromosome Location chr9:139678556-139678557
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139668200-139682400 Weak transcription Right Atrium heart
2 chr9:139673400-139682000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr9:139674800-139678600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr9:139674800-139682000 Weak transcription A549 lung
5 chr9:139675200-139678600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr9:139675400-139682000 Weak transcription Colonic Mucosa Colon
7 chr9:139676000-139678600 Weak transcription Fetal Intestine Large intestine
8 chr9:139676600-139680200 Weak transcription Rectal Mucosa Donor 31 rectum
9 chr9:139676800-139678800 Enhancers Pancreatic Islets Pancreatic Islet
10 chr9:139677600-139679400 Enhancers HepG2 liver
11 chr9:139678400-139678800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr9:139678400-139679200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr9:139678400-139679200 Enhancers K562 blood
14 chr9:139678400-139685000 Enhancers Fetal Intestine Small intestine

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