Variant report

Variant rs7300413
Chromosome Location chr12:66933542-66933543
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:66911400-66938200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr12:66930400-66938000 Weak transcription H9 Cell Line embryonic stem cell
3 chr12:66931000-66933600 Enhancers Fetal Brain Female brain
4 chr12:66932200-66934200 Enhancers Fetal Brain Male brain
5 chr12:66932800-66933600 Enhancers Fetal Intestine Large intestine
6 chr12:66932800-66933600 Enhancers Fetal Intestine Small intestine
7 chr12:66932800-66933800 Enhancers Cortex derived primary cultured neurospheres brain
8 chr12:66932800-66933800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr12:66932800-66934000 Enhancers Brain Substantia Nigra brain
10 chr12:66933000-66933600 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr12:66933000-66933800 Enhancers HUES64 Cell Line embryonic stem cell
12 chr12:66933000-66933800 Enhancers Brain Anterior Caudate brain
13 chr12:66933000-66934000 Enhancers Brain Hippocampus Middle brain
14 chr12:66933200-66934800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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