Variant report

Variant rs9975471
Chromosome Location chr21:46764597-46764598
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46750400-46770200 Weak transcription Gastric stomach
2 chr21:46751600-46769800 Weak transcription Fetal Heart heart
3 chr21:46757200-46764600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr21:46757200-46767400 Weak transcription Right Ventricle heart
5 chr21:46761600-46767000 Weak transcription Spleen Spleen
6 chr21:46761800-46768600 Weak transcription Esophagus oesophagus
7 chr21:46763200-46764800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr21:46764000-46764600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr21:46764000-46765000 Enhancers HepG2 liver
10 chr21:46764200-46764800 Weak transcription Duodenum Mucosa Duodenum
11 chr21:46764200-46764800 Strong transcription Right Atrium heart
12 chr21:46764400-46764600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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