Variant report

Variant rs16922960
Chromosome Location chr9:11458098-11458099
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:11456400-11458800 Enhancers HUES48 Cell Line embryonic stem cell
2 chr9:11457000-11458800 Enhancers Cortex derived primary cultured neurospheres brain
3 chr9:11457200-11458600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr9:11457200-11459000 Enhancers Fetal Heart heart
5 chr9:11457400-11458200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr9:11457400-11458200 Weak transcription Placenta Amnion Placenta Amnion
7 chr9:11457400-11458400 Weak transcription Fetal Brain Female brain
8 chr9:11457600-11458600 Enhancers HUES64 Cell Line embryonic stem cell
9 chr9:11457800-11458200 Weak transcription Fetal Brain Male brain
10 chr9:11457800-11459000 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr9:11458000-11458200 Active TSS Pancreatic Islets Pancreatic Islet
12 chr9:11458000-11458600 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
13 chr9:11458000-11458600 Enhancers Brain Dorsolateral Prefrontal Cortex brain
14 chr9:11458000-11458800 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr9:11458000-11458800 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr9:11458000-11458800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr9:11458000-11458800 Enhancers Fetal Kidney kidney
18 chr9:11458000-11459000 Enhancers HUES6 Cell Line embryonic stem cell
19 chr9:11458000-11459000 Enhancers iPS-15b Cell Line embryonic stem cell

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