Variant report

Variant rs56733441
Chromosome Location chr1:210250492-210250493
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210247600-210253800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr1:210248400-210250600 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr1:210248600-210250600 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr1:210248600-210250600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr1:210248600-210251600 Weak transcription Brain Angular Gyrus brain
6 chr1:210248600-210261000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:210248600-210273200 Weak transcription Fetal Brain Female brain
8 chr1:210250000-210250800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr1:210250000-210251400 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:210250200-210250600 Strong transcription H1 Cell Line embryonic stem cell
11 chr1:210250200-210250600 Strong transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr1:210250400-210263000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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