Variant report

Variant rs788863
Chromosome Location chr4:82132356-82132357
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr4:82129800-82133200 Weak transcription NHLF lung
3 chr4:82130400-82133600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr4:82130600-82133600 Weak transcription Fetal Brain Male brain
5 chr4:82131800-82132800 Weak transcription NHDF-Ad bronchial
6 chr4:82131800-82133600 Weak transcription Fetal Intestine Small intestine
7 chr4:82132000-82132600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr4:82132000-82132800 Weak transcription Fetal Intestine Large intestine
9 chr4:82132000-82135000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:82132200-82132600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr4:82132200-82132800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr4:82132200-82136200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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