Variant report

Variant rs12667763
Chromosome Location chr7:97668012-97668013
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:97663600-97670000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:97664000-97668200 Weak transcription Ovary ovary
3 chr7:97664000-97680400 Weak transcription Spleen Spleen
4 chr7:97666600-97670800 Enhancers Fetal Brain Male brain
5 chr7:97667600-97668400 Active TSS Fetal Brain Female brain
6 chr7:97667800-97668200 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
7 chr7:97667800-97668200 Flanking Active TSS Brain Cingulate Gyrus brain
8 chr7:97667800-97668200 Active TSS Brain Hippocampus Middle brain
9 chr7:97667800-97668200 Bivalent Enhancer HepG2 liver
10 chr7:97667800-97668400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr7:97667800-97668400 Enhancers Cortex derived primary cultured neurospheres brain
12 chr7:97667800-97668400 Active TSS Brain Anterior Caudate brain
13 chr7:97668000-97668200 Active TSS Brain Inferior Temporal Lobe brain
14 chr7:97668000-97668400 Active TSS Right Atrium heart

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