Variant report

Variant rs11159252
Chromosome Location chr14:77677991-77677992
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:77654200-77709400 Weak transcription Esophagus oesophagus
2 chr14:77654600-77679400 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr14:77671000-77679200 Weak transcription Brain Germinal Matrix brain
4 chr14:77671000-77685200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr14:77671000-77686200 Weak transcription Brain Inferior Temporal Lobe brain
6 chr14:77671200-77678600 Weak transcription Fetal Brain Female brain
7 chr14:77671200-77679600 Weak transcription Brain Angular Gyrus brain
8 chr14:77673600-77683400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr14:77674600-77685400 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr14:77674800-77686400 Weak transcription Brain Substantia Nigra brain
11 chr14:77675000-77679200 Weak transcription Brain Anterior Caudate brain
12 chr14:77675200-77678800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr14:77675400-77678200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
14 chr14:77675400-77679000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr14:77675400-77679600 Weak transcription H1 Cell Line embryonic stem cell
16 chr14:77676800-77679400 Enhancers Fetal Adrenal Gland Adrenal Gland
17 chr14:77677600-77679000 Weak transcription Spleen Spleen

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