Variant report

Variant rs58872941
Chromosome Location chr19:43709940-43709941
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43706400-43710000 Weak transcription A549 lung
2 chr19:43708200-43710000 Weak transcription HMEC breast
3 chr19:43709400-43710800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr19:43709600-43710000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr19:43709600-43710200 Enhancers NHEK skin
6 chr19:43709600-43710200 Enhancers Osteobl bone
7 chr19:43709600-43710400 Enhancers Muscle Satellite Cultured Cells --
8 chr19:43709600-43710400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr19:43709600-43712000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr19:43709800-43710200 Flanking Active TSS IMR90 fetal lung fibroblasts Cell Line lung
11 chr19:43709800-43710200 Flanking Active TSS NHLF lung
12 chr19:43709800-43710600 Enhancers NHDF-Ad bronchial
13 chr19:43709800-43711200 Enhancers Placenta Placenta

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