Variant report

Variant rs4663052
Chromosome Location chr2:127636821-127636822
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:127634600-127637000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:127634800-127637200 Weak transcription Gastric stomach
3 chr2:127634800-127637400 Weak transcription H1 Cell Line embryonic stem cell
4 chr2:127636000-127637000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr2:127636400-127643800 Weak transcription Right Atrium heart
6 chr2:127636600-127637200 ZNF genes & repeats Pancreas Pancrea
7 chr2:127636800-127637600 ZNF genes & repeats H9 Cell Line embryonic stem cell
8 chr2:127636800-127637600 ZNF genes & repeats Fetal Kidney kidney
9 chr2:127636800-127637800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr2:127636800-127637800 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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