Variant report

Variant rs16913161
Chromosome Location chr8:50757004-50757005
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:50754000-50757200 Enhancers Fetal Intestine Large intestine
2 chr8:50754200-50757200 Enhancers iPS-20b Cell Line embryonic stem cell
3 chr8:50755000-50757200 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr8:50755200-50757200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr8:50755200-50757200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr8:50755600-50757400 Enhancers HUES64 Cell Line embryonic stem cell
7 chr8:50755800-50757400 Enhancers HUES48 Cell Line embryonic stem cell
8 chr8:50756200-50757200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr8:50756600-50757200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr8:50756600-50758400 Weak transcription Fetal Intestine Small intestine
11 chr8:50757000-50757200 Enhancers H1 Cell Line embryonic stem cell
12 chr8:50757000-50757200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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