Variant report

Variant rs539972051
Chromosome Location chr19:43268975-43268976
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43266600-43269800 Active TSS Placenta Placenta
2 chr19:43267200-43269600 Weak transcription Esophagus oesophagus
3 chr19:43267200-43271000 Weak transcription Pancreas Pancrea
4 chr19:43267800-43269000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr19:43268400-43269800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr19:43268400-43269800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr19:43268600-43269200 Enhancers NHDF-Ad bronchial
8 chr19:43268800-43269000 Enhancers Hela-S3 cervix
9 chr19:43268800-43269000 Enhancers HSMM muscle
10 chr19:43268800-43269000 Enhancers NHLF lung
11 chr19:43268800-43269400 Enhancers Muscle Satellite Cultured Cells --

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