Variant report

Variant rs4983446
Chromosome Location chr14:105039447-105039448
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105030400-105040400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr14:105033400-105046000 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr14:105036600-105046200 Enhancers Fetal Heart heart
4 chr14:105037600-105039600 Bivalent Enhancer Placenta Placenta
5 chr14:105038000-105040200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr14:105038000-105044800 Enhancers Fetal Muscle Leg muscle
7 chr14:105038000-105051000 Enhancers Fetal Intestine Large intestine
8 chr14:105038200-105039600 Enhancers Fetal Brain Female brain
9 chr14:105038200-105040600 Enhancers Fetal Intestine Small intestine
10 chr14:105038400-105040800 Enhancers Left Ventricle heart
11 chr14:105038400-105041400 Enhancers Right Ventricle heart
12 chr14:105039000-105040000 Weak transcription Right Atrium heart
13 chr14:105039000-105040200 Weak transcription Brain Germinal Matrix brain
14 chr14:105039000-105040400 Weak transcription Adipose Nuclei Adipose
15 chr14:105039000-105041400 Strong transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr14:105039200-105039600 Enhancers Fetal Stomach stomach
17 chr14:105039200-105040200 Weak transcription Fetal Brain Male brain
18 chr14:105039200-105040200 Weak transcription Fetal Lung lung
19 chr14:105039400-105044000 Weak transcription Placenta Amnion Placenta Amnion

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