Variant report

Variant rs73321290
Chromosome Location chr12:66930736-66930737
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:66910200-66932800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr12:66911400-66938200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr12:66921000-66933000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr12:66925600-66932200 Weak transcription Fetal Brain Male brain
5 chr12:66926600-66931000 Weak transcription Fetal Brain Female brain
6 chr12:66926600-66932800 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr12:66926600-66933000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr12:66928800-66933000 Weak transcription Pancreas Pancrea
9 chr12:66930400-66933000 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr12:66930400-66933000 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr12:66930400-66938000 Weak transcription H9 Cell Line embryonic stem cell
12 chr12:66930600-66930800 Enhancers Fetal Intestine Small intestine

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