Variant report

Variant rs9973711
Chromosome Location chr2:171635393-171635394
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr2:171630000-171635400 Weak transcription Fetal Intestine Large intestine
4 chr2:171630000-171635800 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr2:171630200-171641800 Weak transcription K562 blood
6 chr2:171634400-171635400 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr2:171634400-171635400 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr2:171634600-171640600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr2:171634800-171635400 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr2:171635200-171635800 Enhancers HUES48 Cell Line embryonic stem cell
11 chr2:171635200-171649800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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