Variant report

Variant rs1296837
Chromosome Location chr14:33181356-33181357
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:33172600-33191600 Weak transcription Psoas Muscle Psoas
2 chr14:33173200-33194800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr14:33177000-33181400 Enhancers Fetal Heart heart
4 chr14:33177800-33181800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr14:33178800-33183200 Weak transcription Aorta Aorta
6 chr14:33178800-33191600 Weak transcription Right Ventricle heart
7 chr14:33179000-33193400 Weak transcription HSMMtube muscle
8 chr14:33180400-33193400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr14:33180600-33186200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
10 chr14:33180600-33191800 Weak transcription Left Ventricle heart
11 chr14:33180600-33193800 Weak transcription Fetal Stomach stomach
12 chr14:33180800-33194600 Weak transcription ES-WA7 Cell Line embryonic stem cell
13 chr14:33181000-33182800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr14:33181000-33183000 Weak transcription Brain Anterior Caudate brain
15 chr14:33181000-33183000 Weak transcription Brain Inferior Temporal Lobe brain
16 chr14:33181000-33188200 Weak transcription Brain Angular Gyrus brain
17 chr14:33181000-33193000 Weak transcription Brain Substantia Nigra brain
18 chr14:33181200-33181600 Weak transcription Brain Hippocampus Middle brain
19 chr14:33181200-33183000 Weak transcription Cortex derived primary cultured neurospheres brain
20 chr14:33181200-33186400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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