Variant report

Variant rs77027630
Chromosome Location chr20:14868832-14868833
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14865400-14869000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr20:14867000-14871000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr20:14868200-14869200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr20:14868200-14869400 Enhancers Dnd41 blood
5 chr20:14868400-14869400 Enhancers Cortex derived primary cultured neurospheres brain
6 chr20:14868600-14869000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr20:14868600-14869000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr20:14868600-14869200 Enhancers Fetal Lung lung
9 chr20:14868800-14869000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr20:14868800-14869200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr20:14868800-14869400 Enhancers Ovary ovary

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