Variant report

Variant rs4943627
Chromosome Location chr13:39677430-39677431
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:39674600-39677800 Enhancers Fetal Brain Male brain
2 chr13:39675800-39679600 Weak transcription HSMMtube muscle
3 chr13:39676000-39680800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr13:39676200-39678200 Enhancers Fetal Brain Female brain
5 chr13:39677000-39677800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr13:39677000-39678000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr13:39677000-39678000 Enhancers Brain Cingulate Gyrus brain
8 chr13:39677000-39678400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
9 chr13:39677000-39678600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr13:39677000-39678600 Enhancers Brain Hippocampus Middle brain
11 chr13:39677000-39678800 Enhancers Brain Substantia Nigra brain
12 chr13:39677200-39677600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr13:39677200-39678000 Enhancers Right Atrium heart
14 chr13:39677200-39678800 Enhancers Fetal Muscle Leg muscle
15 chr13:39677400-39677800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr13:39677400-39677800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr13:39677400-39677800 Flanking Active TSS Brain Inferior Temporal Lobe brain
18 chr13:39677400-39678600 Enhancers Brain Angular Gyrus brain

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