Variant report

Variant rs17079107
Chromosome Location chr6:117710176-117710177
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr6:117708800-117710600 Enhancers HMEC breast
7 chr6:117708800-117713000 Enhancers Fetal Intestine Large intestine
8 chr6:117709000-117712200 Enhancers HepG2 liver
9 chr6:117709200-117711600 Enhancers Fetal Intestine Small intestine
10 chr6:117709400-117710600 Weak transcription Gastric stomach
11 chr6:117709600-117710600 Weak transcription A549 lung
12 chr6:117709600-117713800 Weak transcription Stomach Mucosa stomach
13 chr6:117710000-117711600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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