Variant report

Variant rs55756650
Chromosome Location chr12:39774038-39774039
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:39727000-39779200 Weak transcription Aorta Aorta
2 chr12:39745000-39778600 Weak transcription Pancreas Pancrea
3 chr12:39757000-39784600 Weak transcription Brain Germinal Matrix brain
4 chr12:39761800-39806000 Weak transcription Hela-S3 cervix
5 chr12:39763000-39781400 Weak transcription A549 lung
6 chr12:39764000-39781000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr12:39767400-39784800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:39767600-39791400 Weak transcription GM12878-XiMat blood
9 chr12:39767800-39784800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr12:39768000-39776800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr12:39772200-39778600 Weak transcription Brain Anterior Caudate brain
12 chr12:39772200-39778800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr12:39772400-39780200 Weak transcription Brain Substantia Nigra brain
14 chr12:39772600-39775800 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr12:39772600-39776600 Weak transcription Pancreatic Islets Pancreatic Islet
16 chr12:39772600-39777400 Weak transcription Left Ventricle heart
17 chr12:39772600-39778200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
18 chr12:39772600-39778400 Weak transcription Brain Hippocampus Middle brain
19 chr12:39772800-39778200 Weak transcription Brain Angular Gyrus brain
20 chr12:39772800-39778400 Weak transcription Fetal Heart heart

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