Variant report

Variant rs74078569
Chromosome Location chr12:41127426-41127427
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:41122200-41127600 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr12:41122200-41127800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr12:41122800-41129600 Weak transcription A549 lung
4 chr12:41126000-41127600 Enhancers HUES64 Cell Line embryonic stem cell
5 chr12:41126000-41127600 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr12:41126000-41127800 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr12:41126200-41130000 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr12:41126400-41127800 Enhancers HUES6 Cell Line embryonic stem cell
9 chr12:41126600-41128000 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr12:41126800-41127800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr12:41127000-41127600 Weak transcription Brain Germinal Matrix brain
12 chr12:41127200-41127800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr12:41127200-41128000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr12:41127400-41128400 Flanking Active TSS HUES48 Cell Line embryonic stem cell

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