Variant report

Variant rs55923006
Chromosome Location chr2:171634104-171634105
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171629400-171641000 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr2:171629600-171658800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr2:171630000-171634200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:171630000-171635400 Weak transcription Fetal Intestine Large intestine
5 chr2:171630000-171635800 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr2:171630200-171641800 Weak transcription K562 blood
7 chr2:171633400-171634800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr2:171633600-171634400 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr2:171633800-171634200 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr2:171633800-171634400 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr2:171634000-171634400 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr2:171634000-171634600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr2:171634000-171634800 Enhancers HUES48 Cell Line embryonic stem cell
14 chr2:171634000-171635200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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