Variant report

Variant rs73293856
Chromosome Location chr7:27755786-27755787
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27751200-27756800 Enhancers HepG2 liver
2 chr7:27751400-27756400 Enhancers Fetal Intestine Small intestine
3 chr7:27754000-27756600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:27754400-27755800 Enhancers Brain Hippocampus Middle brain
5 chr7:27754800-27758800 Weak transcription Gastric stomach
6 chr7:27755000-27756000 Enhancers Small Intestine intestine
7 chr7:27755000-27756400 Weak transcription Brain Inferior Temporal Lobe brain
8 chr7:27755000-27756600 Weak transcription Brain Substantia Nigra brain
9 chr7:27755000-27757800 Weak transcription Fetal Lung lung
10 chr7:27755200-27756200 Weak transcription Brain Cingulate Gyrus brain
11 chr7:27755200-27756200 Weak transcription Duodenum Mucosa Duodenum
12 chr7:27755200-27758000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr7:27755200-27762200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr7:27755200-27762800 Weak transcription Brain Angular Gyrus brain
15 chr7:27755400-27757800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr7:27755600-27758800 Weak transcription Fetal Intestine Large intestine

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