Variant report

Variant rs731738
Chromosome Location chr11:33433897-33433898
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33413400-33466200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:33415600-33434000 Weak transcription Fetal Brain Female brain
3 chr11:33423800-33434000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr11:33424000-33440200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr11:33432600-33444000 Weak transcription HSMM muscle
6 chr11:33433000-33435000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:33433200-33434200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
8 chr11:33433400-33434200 Enhancers Brain Cingulate Gyrus brain
9 chr11:33433400-33434800 Enhancers GM12878-XiMat blood
10 chr11:33433400-33435000 Enhancers HSMMtube muscle
11 chr11:33433400-33435400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr11:33433400-33435800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr11:33433400-33442800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr11:33433600-33434600 Enhancers Pancreatic Islets Pancreatic Islet
15 chr11:33433800-33434200 Enhancers Brain Inferior Temporal Lobe brain
16 chr11:33433800-33434400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr11:33433800-33434600 Enhancers Osteobl bone

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