Variant report

Variant rs57619688
Chromosome Location chr21:46447391-46447392
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr21:46446000-46447600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr21:46446600-46447600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr21:46446600-46447600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
9 chr21:46446600-46451400 Weak transcription Ovary ovary
10 chr21:46446800-46447400 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr21:46446800-46447600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr21:46446800-46448600 Weak transcription Fetal Muscle Leg muscle
13 chr21:46446800-46452400 Weak transcription Aorta Aorta
14 chr21:46447000-46447400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr21:46447000-46447600 Enhancers H1 Cell Line embryonic stem cell
16 chr21:46447200-46447400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
17 chr21:46447200-46447400 Enhancers Fetal Lung lung
18 chr21:46447200-46447600 Bivalent Enhancer Fetal Muscle Trunk muscle
19 chr21:46447200-46447600 Flanking Bivalent TSS/Enh HepG2 liver

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