Variant report

Variant rs57778006
Chromosome Location chr14:104901825-104901826
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104888800-104902400 Weak transcription Right Atrium heart
2 chr14:104891800-104902200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr14:104898600-104902200 Weak transcription Ovary ovary
4 chr14:104898800-104902000 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr14:104901000-104902400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:104901200-104902000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr14:104901200-104902200 Weak transcription Brain Germinal Matrix brain
8 chr14:104901200-104904400 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr14:104901400-104902200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr14:104901400-104904800 Enhancers Lung lung
11 chr14:104901800-104902000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr14:104901800-104902200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr14:104901800-104902400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr14:104901800-104902400 Enhancers Pancreas Pancrea
15 chr14:104901800-104903200 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
16 chr14:104901800-104904400 Enhancers Spleen Spleen

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