Variant report

Variant rs58952176
Chromosome Location chr14:71704043-71704044
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:71695800-71709400 Weak transcription Pancreas Pancrea
2 chr14:71699600-71707400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr14:71702800-71706800 Weak transcription Spleen Spleen
4 chr14:71703000-71706800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr14:71703000-71706800 Weak transcription Esophagus oesophagus
6 chr14:71703000-71707200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr14:71703000-71709000 Weak transcription Right Atrium heart
8 chr14:71703200-71704600 Enhancers Cortex derived primary cultured neurospheres brain
9 chr14:71703200-71708600 Weak transcription Brain Cingulate Gyrus brain
10 chr14:71703400-71705400 Weak transcription NHDF-Ad bronchial
11 chr14:71703400-71706800 Weak transcription Fetal Lung lung
12 chr14:71703400-71708400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr14:71703400-71709000 Weak transcription Brain Inferior Temporal Lobe brain
14 chr14:71703600-71706800 Weak transcription Fetal Muscle Leg muscle
15 chr14:71703600-71707200 Weak transcription NHEK skin
16 chr14:71703600-71707400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr14:71704000-71704400 Weak transcription Breast Myoepithelial Primary Cells Breast

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