Variant report

Variant rs13119059
Chromosome Location chr4:9847860-9847861
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9844800-9850600 Weak transcription HepG2 liver
2 chr4:9844800-9851000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:9845000-9851600 Weak transcription Fetal Intestine Small intestine
4 chr4:9845000-9874800 Weak transcription NHEK skin
5 chr4:9847600-9848200 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
6 chr4:9847600-9848200 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
7 chr4:9847800-9848200 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr4:9847800-9848200 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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