Variant report

Variant rs28538733
Chromosome Location chr19:43267786-43267787
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43264600-43268000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
2 chr19:43265200-43267800 Enhancers HSMMtube muscle
3 chr19:43266200-43267800 Enhancers HSMM muscle
4 chr19:43266200-43268000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr19:43266600-43267800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
6 chr19:43266600-43269800 Active TSS Placenta Placenta
7 chr19:43267000-43267800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr19:43267200-43269600 Weak transcription Esophagus oesophagus
9 chr19:43267200-43271000 Weak transcription Pancreas Pancrea
10 chr19:43267400-43268400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr19:43267600-43268600 Weak transcription NHDF-Ad bronchial
12 chr19:43267600-43268600 Weak transcription NHLF lung
13 chr19:43267600-43268800 Weak transcription Muscle Satellite Cultured Cells --
14 chr19:43267600-43268800 Weak transcription Hela-S3 cervix

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