Variant report

Variant rs73043118
Chromosome Location chr6:167381518-167381519
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167371400-167411000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:167373600-167402400 Weak transcription Liver Liver
3 chr6:167373800-167384800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr6:167378800-167398600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr6:167380200-167383000 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr6:167380600-167384200 Weak transcription Fetal Intestine Small intestine
7 chr6:167380800-167382800 Weak transcription NHDF-Ad bronchial
8 chr6:167380800-167383800 Weak transcription Placenta Placenta
9 chr6:167380800-167391000 Weak transcription Osteobl bone
10 chr6:167381200-167384200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr6:167381200-167410000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:167381200-167411000 Weak transcription Fetal Stomach stomach
13 chr6:167381400-167381600 Weak transcription HepG2 liver

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