Variant report

Variant rs62262060
Chromosome Location chr3:49912027-49912028
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:49908000-49913600 Enhancers Fetal Intestine Large intestine
2 chr3:49910000-49912400 Enhancers Stomach Mucosa stomach
3 chr3:49910000-49917200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr3:49910600-49914800 Weak transcription Fetal Lung lung
5 chr3:49910600-49916200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr3:49910800-49914200 Weak transcription Fetal Brain Male brain
7 chr3:49911000-49914200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr3:49911000-49917200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr3:49911200-49914600 Weak transcription Fetal Brain Female brain
10 chr3:49911200-49917200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr3:49911400-49912400 Genic enhancers Fetal Intestine Small intestine
12 chr3:49911800-49918600 Weak transcription Colonic Mucosa Colon
13 chr3:49912000-49912200 Strong transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr3:49912000-49912200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
15 chr3:49912000-49912200 Enhancers Stomach Smooth Muscle stomach
16 chr3:49912000-49919000 Weak transcription Spleen Spleen

Quick Search:


  
Input of quick search could be:

what's new

Quick links