Variant report

Variant rs7664592
Chromosome Location chr4:99722435-99722436
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:99721200-99725000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr4:99721800-99723000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:99722000-99722600 Enhancers Fetal Heart heart
4 chr4:99722000-99723000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
5 chr4:99722000-99723000 Enhancers Left Ventricle heart
6 chr4:99722000-99724600 Enhancers Brain Substantia Nigra brain
7 chr4:99722200-99722800 Enhancers Brain Anterior Caudate brain
8 chr4:99722200-99722800 Enhancers Fetal Intestine Large intestine
9 chr4:99722200-99723000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr4:99722200-99723000 Enhancers Placenta Amnion Placenta Amnion
11 chr4:99722200-99724200 Enhancers Brain Cingulate Gyrus brain
12 chr4:99722400-99722800 Enhancers Brain Angular Gyrus brain
13 chr4:99722400-99722800 Enhancers Brain Hippocampus Middle brain
14 chr4:99722400-99723000 Flanking Active TSS Brain Inferior Temporal Lobe brain
15 chr4:99722400-99723400 Enhancers K562 blood

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