Variant report

Variant rs551053891
Chromosome Location chr10:118856229-118856230
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:118853800-118856400 Enhancers Brain Cingulate Gyrus brain
2 chr10:118853800-118857200 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr10:118854000-118857200 Enhancers Cortex derived primary cultured neurospheres brain
4 chr10:118854000-118857400 Enhancers HUES64 Cell Line embryonic stem cell
5 chr10:118854400-118856600 Enhancers HUES48 Cell Line embryonic stem cell
6 chr10:118854400-118856600 Enhancers Brain Hippocampus Middle brain
7 chr10:118854600-118856400 Enhancers Brain Angular Gyrus brain
8 chr10:118854600-118856400 Enhancers Brain Substantia Nigra brain
9 chr10:118855000-118856400 Weak transcription H1 Cell Line embryonic stem cell
10 chr10:118855000-118856800 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr10:118855000-118860600 Weak transcription Brain Inferior Temporal Lobe brain
12 chr10:118855600-118857400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr10:118855600-118857600 Enhancers Brain Germinal Matrix brain
14 chr10:118856200-118856400 Enhancers ES-WA7 Cell Line embryonic stem cell
15 chr10:118856200-118856400 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr10:118856200-118856600 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
17 chr10:118856200-118857000 Enhancers Fetal Brain Male brain

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