Variant report

Variant rs55706043
Chromosome Location chr14:39715930-39715931
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:39703600-39735400 Weak transcription Pancreas Pancrea
2 chr14:39704400-39734400 Weak transcription Duodenum Mucosa Duodenum
3 chr14:39708800-39718000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:39710000-39717400 Strong transcription HepG2 liver
5 chr14:39710600-39716000 Strong transcription Fetal Intestine Small intestine
6 chr14:39711200-39716000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr14:39711200-39719400 Strong transcription Liver Liver
8 chr14:39711400-39716000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr14:39713400-39716000 Weak transcription Fetal Intestine Large intestine
10 chr14:39713400-39716000 Weak transcription NHEK skin
11 chr14:39715600-39716200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr14:39715600-39717200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr14:39715600-39717200 Enhancers NHDF-Ad bronchial
14 chr14:39715800-39716200 Enhancers Osteobl bone
15 chr14:39715800-39716600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr14:39715800-39716800 Strong transcription Pancreatic Islets Pancreatic Islet
17 chr14:39715800-39717000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
18 chr14:39715800-39717000 Enhancers Muscle Satellite Cultured Cells --
19 chr14:39715800-39717200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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