Variant report

Variant rs549820960
Chromosome Location chr2:112024398-112024399
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:112008600-112048600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:112010600-112024600 Weak transcription HSMMtube muscle
3 chr2:112016600-112029000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:112019200-112032600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr2:112020600-112024600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr2:112020600-112048000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:112022800-112031200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr2:112023400-112046400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr2:112024000-112024400 Enhancers Right Ventricle heart
10 chr2:112024200-112025000 Enhancers Lung lung
11 chr2:112024200-112025200 Enhancers Fetal Lung lung
12 chr2:112024200-112025200 Enhancers Ovary ovary
13 chr2:112024200-112025200 Enhancers Skeletal Muscle Male skeletal muscle
14 chr2:112024200-112025200 Enhancers Skeletal Muscle Female skeletal muscle
15 chr2:112024200-112025400 Enhancers Pancreas Pancrea
16 chr2:112024200-112025600 Enhancers Liver Liver
17 chr2:112024200-112025600 Enhancers Fetal Heart heart

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