Variant report

Variant rs17131593
Chromosome Location chr1:92503338-92503339
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92497000-92525600 Weak transcription Brain Inferior Temporal Lobe brain
2 chr1:92497600-92523400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
3 chr1:92497800-92534200 Weak transcription Dnd41 blood
4 chr1:92502000-92504400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr1:92502600-92503400 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr1:92502600-92503400 Enhancers Fetal Lung lung
7 chr1:92502600-92503600 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr1:92502800-92503400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr1:92502800-92503400 Enhancers HUES48 Cell Line embryonic stem cell
10 chr1:92502800-92503400 Enhancers HUES6 Cell Line embryonic stem cell
11 chr1:92502800-92503400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:92503000-92503400 Enhancers Placenta Amnion Placenta Amnion
13 chr1:92503000-92503600 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
14 chr1:92503200-92504000 Weak transcription Fetal Intestine Large intestine
15 chr1:92503200-92505000 Enhancers Fetal Intestine Small intestine

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