Variant report

Variant rs72905021
Chromosome Location chr11:45494608-45494609
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45490200-45495200 Weak transcription H1 Cell Line embryonic stem cell
2 chr11:45490200-45495200 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr11:45490200-45510800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr11:45490400-45495000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr11:45490400-45495000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr11:45494200-45499400 Enhancers Fetal Brain Male brain
7 chr11:45494600-45494800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr11:45494600-45494800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
9 chr11:45494600-45494800 Bivalent Enhancer Fetal Intestine Small intestine
10 chr11:45494600-45495000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr11:45494600-45495400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr11:45494600-45495600 Enhancers Fetal Muscle Trunk muscle
13 chr11:45494600-45495600 Bivalent Enhancer Fetal Stomach stomach
14 chr11:45494600-45495600 Enhancers Pancreas Pancrea
15 chr11:45494600-45495800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr11:45494600-45496200 Enhancers Fetal Brain Female brain

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