Variant report

Variant rs201389233
Chromosome Location chr21:46442547-46442548
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46438200-46442600 Bivalent Enhancer Fetal Muscle Trunk muscle
2 chr21:46438600-46453000 Weak transcription Placenta Amnion Placenta Amnion
3 chr21:46439400-46443400 Weak transcription Fetal Heart heart
4 chr21:46439400-46452200 Weak transcription Esophagus oesophagus
5 chr21:46439800-46442800 Enhancers Placenta Placenta
6 chr21:46439800-46443000 Enhancers HepG2 liver
7 chr21:46440000-46442600 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr21:46440200-46442800 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
9 chr21:46440400-46446000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr21:46440600-46449200 Weak transcription Right Atrium heart
11 chr21:46441600-46449400 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr21:46442200-46442800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr21:46442200-46450800 Weak transcription Spleen Spleen
14 chr21:46442400-46446000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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