Variant report

Variant rs2256786
Chromosome Location chr9:15371307-15371308
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15369000-15374800 Enhancers Fetal Lung lung
2 chr9:15370400-15371800 Enhancers Cortex derived primary cultured neurospheres brain
3 chr9:15370600-15371600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
4 chr9:15370600-15373000 Enhancers Ovary ovary
5 chr9:15370800-15371400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr9:15370800-15374600 Enhancers Fetal Intestine Large intestine
7 chr9:15371000-15371400 Flanking Active TSS Brain Dorsolateral Prefrontal Cortex brain
8 chr9:15371000-15371400 Enhancers Rectal Mucosa Donor 29 rectum
9 chr9:15371000-15371400 Flanking Active TSS HepG2 liver
10 chr9:15371000-15372800 Enhancers Sigmoid Colon Sigmoid Colon
11 chr9:15371000-15373400 Enhancers Fetal Intestine Small intestine
12 chr9:15371000-15375000 Enhancers Rectal Mucosa Donor 31 rectum
13 chr9:15371200-15371400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr9:15371200-15371600 Enhancers Stomach Mucosa stomach
15 chr9:15371200-15372400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr9:15371200-15372600 Enhancers Colonic Mucosa Colon
17 chr9:15371200-15373600 Weak transcription Placenta Placenta

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