Variant report

Variant rs10124011
Chromosome Location chr9:139678796-139678797
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr9:139674800-139682000 Weak transcription A549 lung
4 chr9:139675400-139682000 Weak transcription Colonic Mucosa Colon
5 chr9:139676600-139680200 Weak transcription Rectal Mucosa Donor 31 rectum
6 chr9:139676800-139678800 Enhancers Pancreatic Islets Pancreatic Islet
7 chr9:139677600-139679400 Enhancers HepG2 liver
8 chr9:139678400-139678800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr9:139678400-139679200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr9:139678400-139679200 Enhancers K562 blood
11 chr9:139678400-139685000 Enhancers Fetal Intestine Small intestine
12 chr9:139678600-139678800 Enhancers Brain Substantia Nigra brain
13 chr9:139678600-139678800 Enhancers Rectal Mucosa Donor 29 rectum
14 chr9:139678600-139679200 Enhancers Brain Anterior Caudate brain
15 chr9:139678600-139679200 Enhancers Brain Hippocampus Middle brain
16 chr9:139678600-139679800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr9:139678600-139679800 Enhancers Primary hematopoietic stem cells short term culture blood
18 chr9:139678600-139680400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
19 chr9:139678600-139683000 Enhancers Fetal Intestine Large intestine

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