Variant report

Variant rs9480947
Chromosome Location chr6:109718565-109718566
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109705000-109745200 Weak transcription Fetal Kidney kidney
2 chr6:109706600-109735800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr6:109706800-109718600 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr6:109707000-109755400 Weak transcription Fetal Intestine Small intestine
5 chr6:109711800-109725000 Weak transcription Brain Anterior Caudate brain
6 chr6:109712800-109736200 Weak transcription Left Ventricle heart
7 chr6:109715200-109721600 Weak transcription K562 blood
8 chr6:109715400-109730400 Weak transcription Brain Hippocampus Middle brain
9 chr6:109716200-109723600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr6:109716600-109719000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr6:109717000-109718800 Enhancers Primary monocytes fromperipheralblood blood
12 chr6:109717200-109718800 Enhancers Monocytes-CD14+_RO01746 blood
13 chr6:109718000-109721800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr6:109718400-109718800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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