Variant report

Variant rs45619837
Chromosome Location chr2:171687349-171687350
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171679600-171688800 Weak transcription K562 blood
2 chr2:171680200-171688800 Weak transcription NHDF-Ad bronchial
3 chr2:171681200-171693800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr2:171682200-171691600 Genic enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:171683400-171688800 Strong transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr2:171683600-171694200 Genic enhancers Cortex derived primary cultured neurospheres brain
7 chr2:171685400-171689000 Strong transcription Brain Germinal Matrix brain
8 chr2:171685600-171692600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:171685800-171699000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:171686400-171687400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr2:171686400-171699200 Strong transcription HUES6 Cell Line embryonic stem cell
12 chr2:171686800-171687800 Strong transcription Aorta Aorta
13 chr2:171687200-171687800 Strong transcription Brain Anterior Caudate brain

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