Variant report

Variant rs36023624
Chromosome Location chr11:58830430-58830431
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58830000-58830600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
2 chr11:58830000-58830600 Bivalent/Poised TSS Fetal Brain Female brain
3 chr11:58830000-58830600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr11:58830000-58830600 Enhancers Pancreas Pancrea
5 chr11:58830200-58830600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:58830200-58830600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:58830200-58830600 Bivalent Enhancer Brain Cingulate Gyrus brain
8 chr11:58830200-58830600 Bivalent/Poised TSS Brain Germinal Matrix brain
9 chr11:58830200-58830800 Active TSS Brain Inferior Temporal Lobe brain
10 chr11:58830400-58830600 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:58830400-58830600 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
12 chr11:58830400-58830600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
13 chr11:58830400-58830600 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr11:58830400-58830800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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