Variant report

Variant rs171442
Chromosome Location chr17:43891906-43891907
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43889600-43892800 Enhancers Brain Anterior Caudate brain
2 chr17:43889800-43892800 Enhancers Brain Hippocampus Middle brain
3 chr17:43889800-43892800 Enhancers Brain Substantia Nigra brain
4 chr17:43889800-43893600 Enhancers Brain Inferior Temporal Lobe brain
5 chr17:43890000-43892200 Enhancers Brain Angular Gyrus brain
6 chr17:43890600-43892600 Enhancers Brain Cingulate Gyrus brain
7 chr17:43891200-43892400 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr17:43891200-43892400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
9 chr17:43891200-43896000 Weak transcription Fetal Brain Male brain
10 chr17:43891200-43902400 Weak transcription Brain Germinal Matrix brain
11 chr17:43891600-43894200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr17:43891600-43894400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr17:43891800-43892400 Enhancers Fetal Brain Female brain
14 chr17:43891800-43892800 Enhancers Fetal Muscle Trunk muscle
15 chr17:43891800-43894400 Bivalent Enhancer HepG2 liver

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