Variant report

Variant rs569071720
Chromosome Location chr1:228234339-228234340
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:228231400-228239600 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr1:228232800-228234600 Enhancers Esophagus oesophagus
3 chr1:228232800-228234600 Enhancers Gastric stomach
4 chr1:228232800-228234600 Enhancers Lung lung
5 chr1:228233800-228234400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:228234000-228234400 Bivalent Enhancer H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:228234000-228234400 ZNF genes & repeats H9 Cell Line embryonic stem cell
8 chr1:228234000-228234400 Bivalent Enhancer Fetal Lung lung
9 chr1:228234000-228234600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:228234000-228234600 Enhancers Pancreas Pancrea
11 chr1:228234200-228234600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
12 chr1:228234200-228235800 Weak transcription Stomach Mucosa stomach

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