Variant report

Variant rs4902648
Chromosome Location chr14:39903613-39903614
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:39902400-39910200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr14:39902400-39911400 Weak transcription Gastric stomach
3 chr14:39902800-39910200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr14:39903000-39910000 Weak transcription Lung lung
5 chr14:39903000-39910800 Weak transcription Fetal Brain Male brain
6 chr14:39903000-39911200 Weak transcription Brain Inferior Temporal Lobe brain
7 chr14:39903000-39912600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr14:39903000-39916400 Weak transcription Fetal Heart heart
9 chr14:39903200-39904000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr14:39903200-39904000 Enhancers Muscle Satellite Cultured Cells --
11 chr14:39903200-39904400 Weak transcription Brain Anterior Caudate brain
12 chr14:39903200-39910800 Weak transcription Brain Hippocampus Middle brain
13 chr14:39903200-39912000 Weak transcription Aorta Aorta
14 chr14:39903400-39904000 Enhancers HepG2 liver
15 chr14:39903400-39904400 Enhancers GM12878-XiMat blood
16 chr14:39903400-39904400 Enhancers Hela-S3 cervix
17 chr14:39903600-39904000 Enhancers Pancreatic Islets Pancreatic Islet

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