Variant report

Variant rs6976828
Chromosome Location chr7:4066500-4066501
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4059000-4067000 Weak transcription Right Ventricle heart
2 chr7:4059000-4091200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr7:4061400-4067000 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr7:4061400-4073200 Weak transcription Fetal Lung lung
5 chr7:4061400-4080800 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr7:4064600-4067800 Weak transcription Fetal Intestine Small intestine
7 chr7:4064800-4066800 Strong transcription Pancreas Pancrea
8 chr7:4065600-4077000 Weak transcription Aorta Aorta
9 chr7:4066000-4066600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr7:4066000-4066600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr7:4066000-4069800 Weak transcription Colon Smooth Muscle Colon
12 chr7:4066200-4066600 Strong transcription Fetal Stomach stomach
13 chr7:4066200-4067800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr7:4066400-4066800 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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