Variant report

Variant rs55847910
Chromosome Location chr8:49334732-49334733
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49331200-49334800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr8:49332200-49335000 Weak transcription Fetal Stomach stomach
3 chr8:49332400-49340200 Weak transcription Fetal Intestine Small intestine
4 chr8:49332800-49338600 Weak transcription Spleen Spleen
5 chr8:49333000-49335200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr8:49333400-49339800 Weak transcription Pancreas Pancrea
7 chr8:49333800-49341400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr8:49334000-49335200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr8:49334000-49339800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr8:49334200-49335200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr8:49334200-49339800 Weak transcription Right Atrium heart
12 chr8:49334400-49339200 Weak transcription Fetal Brain Female brain
13 chr8:49334400-49339800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr8:49334400-49339800 Weak transcription Fetal Lung lung
15 chr8:49334600-49335000 Enhancers Fetal Brain Male brain
16 chr8:49334600-49339400 Weak transcription NHDF-Ad bronchial
17 chr8:49334600-49339800 Weak transcription Muscle Satellite Cultured Cells --
18 chr8:49334600-49339800 Weak transcription NHLF lung

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