Variant report

Variant rs72965321
Chromosome Location chr6:117709381-117709382
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr6:117707000-117709600 Enhancers Stomach Mucosa stomach
5 chr6:117707400-117715800 Weak transcription HSMM muscle
6 chr6:117708000-117714200 Enhancers Liver Liver
7 chr6:117708600-117709600 Enhancers A549 lung
8 chr6:117708800-117709400 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:117708800-117709400 Enhancers Pancreas Pancrea
10 chr6:117708800-117710600 Enhancers HMEC breast
11 chr6:117708800-117713000 Enhancers Fetal Intestine Large intestine
12 chr6:117709000-117709400 Enhancers Gastric stomach
13 chr6:117709000-117712200 Enhancers HepG2 liver
14 chr6:117709200-117711600 Enhancers Fetal Intestine Small intestine

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