Variant report

Variant rs12300722
Chromosome Location chr12:8829136-8829137
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:8811800-8829600 Weak transcription Thymus Thymus
2 chr12:8821600-8845000 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr12:8824000-8833600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr12:8827600-8829400 Enhancers HUVEC blood vessel
5 chr12:8827800-8829600 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr12:8827800-8829800 Enhancers Adipose Nuclei Adipose
7 chr12:8828000-8829600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr12:8828000-8830000 Enhancers Primary T cells from cord blood blood
9 chr12:8828000-8833400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr12:8828400-8829400 Weak transcription Hela-S3 cervix
11 chr12:8828400-8830000 Enhancers Fetal Thymus thymus
12 chr12:8828400-8833800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr12:8828400-8840400 Weak transcription Brain Anterior Caudate brain
14 chr12:8828600-8829600 Weak transcription ES-I3 Cell Line embryonic stem cell
15 chr12:8828600-8834000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr12:8828800-8833600 Weak transcription Fetal Intestine Small intestine
17 chr12:8828800-8833800 Weak transcription Fetal Kidney kidney
18 chr12:8828800-8837200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
19 chr12:8829000-8829200 Weak transcription Left Ventricle heart

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