Variant report

Variant rs62055475
Chromosome Location chr17:43945106-43945107
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43942400-43947400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr17:43942800-43946200 Enhancers Brain Hippocampus Middle brain
3 chr17:43942800-43946400 Enhancers Brain Substantia Nigra brain
4 chr17:43943000-43946200 Enhancers Brain Cingulate Gyrus brain
5 chr17:43943400-43947200 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr17:43943400-43947400 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr17:43943600-43947400 Weak transcription ES-WA7 Cell Line embryonic stem cell
8 chr17:43944000-43947800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr17:43944200-43945600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr17:43944400-43945400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr17:43944800-43946200 Enhancers Brain Inferior Temporal Lobe brain
12 chr17:43944800-43946400 Enhancers Brain Anterior Caudate brain
13 chr17:43945000-43945200 Flanking Bivalent TSS/Enh HepG2 liver
14 chr17:43945000-43946400 Enhancers Brain Angular Gyrus brain
15 chr17:43945000-43947400 Weak transcription Cortex derived primary cultured neurospheres brain

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