Variant report

Variant rs11004933
Chromosome Location chr10:57388898-57388899
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:57388400-57389000 Bivalent/Poised TSS Fetal Kidney kidney
2 chr10:57388400-57389600 Weak transcription Pancreas Pancrea
3 chr10:57388400-57390000 Weak transcription Gastric stomach
4 chr10:57388600-57389000 Bivalent Enhancer Fetal Heart heart
5 chr10:57388600-57389600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr10:57388600-57389600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr10:57388600-57389600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr10:57388600-57389600 Weak transcription Right Atrium heart
9 chr10:57388600-57390200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr10:57388800-57389000 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
11 chr10:57388800-57389000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
12 chr10:57388800-57389000 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
13 chr10:57388800-57389000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
14 chr10:57388800-57389000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
15 chr10:57388800-57389600 Weak transcription Right Ventricle heart

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