Variant report

Variant rs535405430
Chromosome Location chr5:117893265-117893266
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:117885200-117894200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr5:117889600-117894600 Weak transcription Right Atrium heart
3 chr5:117890200-117894400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr5:117890600-117893400 Weak transcription Muscle Satellite Cultured Cells --
5 chr5:117890800-117894200 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr5:117891800-117894200 Weak transcription Pancreatic Islets Pancreatic Islet
7 chr5:117891800-117895000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr5:117892000-117894400 Enhancers Fetal Lung lung
9 chr5:117892600-117893600 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr5:117892600-117894000 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr5:117892600-117894600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr5:117892600-117894800 Weak transcription Fetal Heart heart
13 chr5:117892600-117895200 Enhancers HMEC breast
14 chr5:117892600-117896000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr5:117892800-117893800 Enhancers Fetal Muscle Leg muscle
16 chr5:117892800-117894600 Enhancers NHLF lung
17 chr5:117892800-117895200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr5:117893000-117893400 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
19 chr5:117893000-117893800 Enhancers Placenta Placenta
20 chr5:117893000-117895200 Enhancers NHDF-Ad bronchial
21 chr5:117893200-117893400 Enhancers Osteobl bone
22 chr5:117893200-117894600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
23 chr5:117893200-117895600 Weak transcription Left Ventricle heart

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