Variant report

Variant rs11904031
Chromosome Location chr2:211409732-211409733
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:211405000-211409800 Enhancers Fetal Intestine Large intestine
2 chr2:211406000-211413800 Weak transcription H9 Cell Line embryonic stem cell
3 chr2:211406200-211413600 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr2:211406200-211421000 Weak transcription H1 Cell Line embryonic stem cell
5 chr2:211406400-211411000 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr2:211406400-211411600 Weak transcription Brain Hippocampus Middle brain
7 chr2:211406600-211411400 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr2:211406600-211411400 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr2:211406600-211411400 Weak transcription Brain Substantia Nigra brain
10 chr2:211406600-211412800 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr2:211406600-211413000 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr2:211409200-211409800 Weak transcription Fetal Intestine Small intestine
13 chr2:211409400-211409800 Enhancers Duodenum Mucosa Duodenum
14 chr2:211409600-211410000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr2:211409600-211410000 Enhancers HepG2 liver
16 chr2:211409600-211412400 Enhancers Liver Liver

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