Variant report

Variant rs4743279
Chromosome Location chr9:101560358-101560359
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:101558400-101563800 Weak transcription Fetal Brain Male brain
2 chr9:101559400-101561800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:101559400-101562000 Weak transcription Aorta Aorta
4 chr9:101559400-101562200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr9:101559400-101564000 Weak transcription K562 blood
6 chr9:101559600-101561800 Weak transcription H9 Cell Line embryonic stem cell
7 chr9:101559600-101562200 Weak transcription Osteobl bone
8 chr9:101559600-101564000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr9:101559600-101564200 Weak transcription Colon Smooth Muscle Colon
10 chr9:101559600-101565200 Weak transcription Esophagus oesophagus
11 chr9:101559600-101567600 Weak transcription Stomach Smooth Muscle stomach
12 chr9:101559600-101567800 Weak transcription Stomach Mucosa stomach
13 chr9:101559600-101569000 Weak transcription Pancreas Pancrea
14 chr9:101559600-101569600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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