Variant report

Variant rs73380566
Chromosome Location chr21:46446883-46446884
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46438600-46453000 Weak transcription Placenta Amnion Placenta Amnion
2 chr21:46439400-46452200 Weak transcription Esophagus oesophagus
3 chr21:46440600-46449200 Weak transcription Right Atrium heart
4 chr21:46441600-46449400 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr21:46442200-46450800 Weak transcription Spleen Spleen
6 chr21:46446000-46447200 Enhancers Fetal Muscle Trunk muscle
7 chr21:46446000-46447600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr21:46446600-46447200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr21:46446600-46447200 Genic enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr21:46446600-46447600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr21:46446600-46447600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
12 chr21:46446600-46451400 Weak transcription Ovary ovary
13 chr21:46446800-46447200 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
14 chr21:46446800-46447400 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr21:46446800-46447600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr21:46446800-46448600 Weak transcription Fetal Muscle Leg muscle
17 chr21:46446800-46452400 Weak transcription Aorta Aorta

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