Variant report

Variant rs17562100
Chromosome Location chr2:50999907-50999908
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50992800-51000800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr2:50993000-51000800 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr2:50995000-51000600 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr2:50996400-51000800 Weak transcription Brain Cingulate Gyrus brain
5 chr2:50997000-51001400 Enhancers Liver Liver
6 chr2:50997200-51000800 Weak transcription Brain Anterior Caudate brain
7 chr2:50997200-51000800 Weak transcription Brain Substantia Nigra brain
8 chr2:50998000-51000800 Enhancers Duodenum Mucosa Duodenum
9 chr2:50998000-51001200 Enhancers Fetal Intestine Large intestine
10 chr2:50998200-51001000 Enhancers Fetal Intestine Small intestine
11 chr2:50998800-51001600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr2:50999000-51000000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr2:50999200-51000000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
14 chr2:50999200-51000000 Enhancers Small Intestine intestine
15 chr2:50999600-51001000 Enhancers Pancreatic Islets Pancreatic Islet
16 chr2:50999800-51000000 Enhancers HUES48 Cell Line embryonic stem cell
17 chr2:50999800-51001200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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