Variant report

Variant rs57847806
Chromosome Location chr12:39770676-39770677
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:39697800-39771800 Weak transcription Fetal Kidney kidney
2 chr12:39727000-39779200 Weak transcription Aorta Aorta
3 chr12:39745000-39778600 Weak transcription Pancreas Pancrea
4 chr12:39751600-39771800 Weak transcription Brain Anterior Caudate brain
5 chr12:39757000-39784600 Weak transcription Brain Germinal Matrix brain
6 chr12:39761800-39806000 Weak transcription Hela-S3 cervix
7 chr12:39762800-39771200 Weak transcription Pancreatic Islets Pancreatic Islet
8 chr12:39763000-39781400 Weak transcription A549 lung
9 chr12:39764000-39781000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr12:39765800-39772200 Weak transcription Left Ventricle heart
11 chr12:39767400-39770800 Weak transcription Right Ventricle heart
12 chr12:39767400-39784800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:39767600-39791400 Weak transcription GM12878-XiMat blood
14 chr12:39767800-39771000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr12:39767800-39784800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr12:39768000-39776800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
17 chr12:39769200-39771800 Weak transcription Brain Angular Gyrus brain
18 chr12:39769800-39771400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
19 chr12:39770000-39772200 Weak transcription Fetal Heart heart
20 chr12:39770400-39772600 Enhancers Cortex derived primary cultured neurospheres brain
21 chr12:39770600-39771000 Enhancers Brain Inferior Temporal Lobe brain
22 chr12:39770600-39771400 Weak transcription Brain Hippocampus Middle brain

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