Variant report

Variant rs373982103
Chromosome Location chr20:14869098-14869099
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14867000-14871000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr20:14868200-14869200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr20:14868200-14869400 Enhancers Dnd41 blood
4 chr20:14868400-14869400 Enhancers Cortex derived primary cultured neurospheres brain
5 chr20:14868600-14869200 Enhancers Fetal Lung lung
6 chr20:14868800-14869200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr20:14868800-14869400 Enhancers Ovary ovary
8 chr20:14869000-14869200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr20:14869000-14869200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr20:14869000-14869400 Enhancers Colon Smooth Muscle Colon
11 chr20:14869000-14869400 Enhancers Fetal Heart heart

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