Variant report

Variant rs16913859
Chromosome Location chr8:50829883-50829884
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:50824600-50831600 Weak transcription H9 Cell Line embryonic stem cell
2 chr8:50824800-50830000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr8:50825000-50831800 Weak transcription H1 Cell Line embryonic stem cell
4 chr8:50826600-50830000 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr8:50826800-50830000 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr8:50826800-50830000 Weak transcription Brain Inferior Temporal Lobe brain
7 chr8:50828200-50833800 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr8:50828400-50830000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr8:50828600-50831200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr8:50828600-50836000 Weak transcription Fetal Brain Female brain
11 chr8:50828800-50834200 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr8:50829600-50830000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr8:50829800-50830200 Active TSS iPS-20b Cell Line embryonic stem cell
14 chr8:50829800-50830200 Enhancers Brain Germinal Matrix brain
15 chr8:50829800-50830600 Enhancers HUES6 Cell Line embryonic stem cell
16 chr8:50829800-50830800 Enhancers iPS-15b Cell Line embryonic stem cell
17 chr8:50829800-50832000 Enhancers ES-I3 Cell Line embryonic stem cell
18 chr8:50829800-50833400 Enhancers HUES64 Cell Line embryonic stem cell

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