Variant report

Variant rs58874817
Chromosome Location chr11:33500539-33500540
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33494400-33503200 Enhancers Fetal Brain Male brain
2 chr11:33495000-33502600 Enhancers Brain Germinal Matrix brain
3 chr11:33495800-33502400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
4 chr11:33496000-33502800 Enhancers Cortex derived primary cultured neurospheres brain
5 chr11:33497000-33500800 Enhancers Fetal Intestine Small intestine
6 chr11:33497200-33501000 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr11:33497200-33502200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr11:33498200-33500800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr11:33498200-33501200 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr11:33498200-33502400 Weak transcription Brain Angular Gyrus brain
11 chr11:33499600-33500600 Enhancers Liver Liver
12 chr11:33499600-33502200 Weak transcription Pancreas Pancrea
13 chr11:33499800-33500800 Weak transcription Brain Anterior Caudate brain
14 chr11:33500000-33501600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr11:33500000-33501800 Weak transcription Brain Inferior Temporal Lobe brain
16 chr11:33500200-33500800 Enhancers Fetal Brain Female brain
17 chr11:33500200-33501200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
18 chr11:33500200-33503000 Weak transcription Pancreatic Islets Pancreatic Islet
19 chr11:33500200-33505400 Weak transcription H9 Cell Line embryonic stem cell

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