Variant report

Variant rs17084432
Chromosome Location chr4:55391919-55391920
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:55390600-55393200 Enhancers Placenta Placenta
2 chr4:55391400-55392400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr4:55391400-55392600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr4:55391400-55392600 Enhancers NHLF lung
5 chr4:55391400-55392800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr4:55391400-55392800 Enhancers NHDF-Ad bronchial
7 chr4:55391400-55392800 Enhancers NHEK skin
8 chr4:55391400-55393000 Enhancers HMEC breast
9 chr4:55391600-55392000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr4:55391600-55392400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr4:55391600-55392400 Enhancers K562 blood
12 chr4:55391600-55392600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr4:55391600-55392600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:55391600-55392600 Enhancers Osteobl bone
15 chr4:55391600-55392800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr4:55391600-55393400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr4:55391800-55392400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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