Variant report

Variant rs61246559
Chromosome Location chr2:171580370-171580371
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171574600-171585600 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr2:171577800-171586200 Weak transcription Fetal Intestine Large intestine
4 chr2:171578800-171580400 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr2:171579800-171580400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr2:171580000-171580400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr2:171580000-171580400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr2:171580000-171580600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr2:171580200-171580400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:171580200-171580400 Enhancers Fetal Lung lung
11 chr2:171580200-171589600 Weak transcription Fetal Intestine Small intestine

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