Variant report

Variant rs10779928
Chromosome Location chr2:40221899-40221900
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40218200-40222600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr2:40218400-40225200 Weak transcription Fetal Kidney kidney
3 chr2:40219000-40223600 Weak transcription HSMMtube muscle
4 chr2:40219000-40223800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr2:40219200-40224400 Weak transcription Osteobl bone
6 chr2:40220800-40225000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:40220800-40225200 Enhancers HMEC breast
8 chr2:40221000-40222000 Enhancers Muscle Satellite Cultured Cells --
9 chr2:40221000-40225000 Enhancers NHEK skin
10 chr2:40221400-40222000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:40221400-40225000 Enhancers HSMM muscle
12 chr2:40221400-40225200 Enhancers Dnd41 blood
13 chr2:40221800-40222000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr2:40221800-40223600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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