Variant report

Variant rs538323569
Chromosome Location chr20:14987529-14987530
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14986200-14991000 Weak transcription Fetal Kidney kidney
2 chr20:14986400-14990600 Weak transcription Fetal Intestine Large intestine
3 chr20:14986600-14992600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr20:14986600-14993400 Weak transcription HepG2 liver
5 chr20:14986600-14996400 Weak transcription Ovary ovary
6 chr20:14987000-14988600 Enhancers Cortex derived primary cultured neurospheres brain
7 chr20:14987400-14987800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr20:14987400-14988600 Enhancers Breast Myoepithelial Primary Cells Breast

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