Variant report

Variant rs17079119
Chromosome Location chr6:117713312-117713313
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:117662000-117717200 Weak transcription HSMMtube muscle
2 chr6:117692600-117735800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr6:117692800-117717400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr6:117707400-117715800 Weak transcription HSMM muscle
5 chr6:117708000-117714200 Enhancers Liver Liver
6 chr6:117709600-117713800 Weak transcription Stomach Mucosa stomach
7 chr6:117711400-117714000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:117711600-117713800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:117711600-117713800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr6:117711600-117714000 Weak transcription NHEK skin
11 chr6:117712600-117713800 Enhancers HepG2 liver
12 chr6:117713000-117713400 Weak transcription HMEC breast

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