Variant report

Variant rs6962378
Chromosome Location chr7:17678165-17678166
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17670600-17686000 Weak transcription Osteobl bone
2 chr7:17673000-17678200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:17673200-17678200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17673400-17678400 Weak transcription NHDF-Ad bronchial
5 chr7:17677600-17679600 Enhancers NHEK skin
6 chr7:17677800-17679000 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr7:17678000-17678800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr7:17678000-17678800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr7:17678000-17679000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr7:17678000-17679800 Enhancers HMEC breast

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