Variant report

Variant rs10129362
Chromosome Location chr14:32846235-32846236
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32836600-32846800 Weak transcription Fetal Brain Male brain
2 chr14:32843400-32846600 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr14:32843600-32846600 Weak transcription Brain Anterior Caudate brain
4 chr14:32843600-32848600 Weak transcription K562 blood
5 chr14:32843800-32846400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr14:32843800-32848400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr14:32843800-32849000 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr14:32845200-32851000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr14:32845400-32846800 Weak transcription HMEC breast
10 chr14:32845400-32847200 Enhancers Brain Hippocampus Middle brain
11 chr14:32845400-32847800 Enhancers Brain Cingulate Gyrus brain
12 chr14:32845400-32848600 Weak transcription NHEK skin
13 chr14:32845600-32848600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr14:32846200-32846400 Enhancers Brain Inferior Temporal Lobe brain
15 chr14:32846200-32846600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
16 chr14:32846200-32847200 Enhancers Brain Angular Gyrus brain
17 chr14:32846200-32848000 Enhancers Brain Substantia Nigra brain

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