Variant report

Variant rs200384560
Chromosome Location chr21:46766060-46766061
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr21:46757200-46767400 Weak transcription Right Ventricle heart
4 chr21:46761600-46767000 Weak transcription Spleen Spleen
5 chr21:46761800-46768600 Weak transcription Esophagus oesophagus
6 chr21:46764600-46766200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr21:46764800-46767600 Weak transcription Right Atrium heart
8 chr21:46765000-46767200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr21:46765000-46767600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr21:46765000-46770000 Weak transcription Duodenum Mucosa Duodenum
11 chr21:46765200-46767200 Weak transcription NHDF-Ad bronchial

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