Variant report

Variant rs2044211
Chromosome Location chr4:82134287-82134288
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:82126800-82134800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr4:82132000-82135000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:82132200-82136200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr4:82132800-82135400 Active TSS Fetal Intestine Large intestine
5 chr4:82133200-82136000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr4:82133400-82134400 Weak transcription NHLF lung
7 chr4:82133400-82134600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr4:82133600-82134600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr4:82133600-82134800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr4:82133600-82135200 Active TSS Fetal Intestine Small intestine
11 chr4:82134000-82134800 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
12 chr4:82134200-82134400 Bivalent/Poised TSS Fetal Brain Male brain
13 chr4:82134200-82134600 Active TSS Fetal Brain Female brain
14 chr4:82134200-82135400 Bivalent/Poised TSS Primary T cells from cord blood blood
15 chr4:82134200-82136600 Active TSS NHDF-Ad bronchial

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