Variant report

Variant rs6939342
Chromosome Location chr6:145695363-145695364
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145693200-145695400 Enhancers Stomach Mucosa stomach
2 chr6:145694000-145696000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:145694400-145698600 Weak transcription Aorta Aorta
4 chr6:145694400-145698800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:145695000-145696200 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr6:145695000-145698600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr6:145695200-145695600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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