Variant report

Variant rs28398007
Chromosome Location chr14:67446561-67446562
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67414800-67480000 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr14:67415600-67486400 Weak transcription Pancreas Pancrea
3 chr14:67416400-67491200 Weak transcription Left Ventricle heart
4 chr14:67418000-67491400 Weak transcription Ovary ovary
5 chr14:67424800-67456000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr14:67424800-67499000 Weak transcription Aorta Aorta
7 chr14:67427000-67460800 Weak transcription Duodenum Mucosa Duodenum
8 chr14:67427400-67453000 Weak transcription Psoas Muscle Psoas
9 chr14:67427600-67464800 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr14:67427600-67498800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr14:67427800-67459200 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr14:67428000-67454000 Weak transcription Primary hematopoietic stem cells blood
13 chr14:67429800-67469600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
14 chr14:67432600-67454600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr14:67438000-67491400 Weak transcription Fetal Intestine Small intestine
16 chr14:67444800-67447000 Strong transcription Liver Liver
17 chr14:67445800-67446600 Enhancers GM12878-XiMat blood
18 chr14:67446200-67474600 Weak transcription Fetal Kidney kidney

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