Variant report

Variant rs10281729
Chromosome Location chr7:17672844-17672845
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17670600-17686000 Weak transcription Osteobl bone
2 chr7:17671600-17673200 Enhancers Hela-S3 cervix
3 chr7:17672400-17673000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:17672400-17673000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr7:17672400-17673000 Enhancers HMEC breast
6 chr7:17672400-17673200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr7:17672400-17673200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr7:17672400-17673200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:17672400-17673200 Enhancers Muscle Satellite Cultured Cells --
10 chr7:17672400-17673200 Enhancers NHEK skin
11 chr7:17672400-17673200 Enhancers NHLF lung
12 chr7:17672400-17673400 Enhancers Primary monocytes fromperipheralblood blood
13 chr7:17672400-17673400 Enhancers Monocytes-CD14+_RO01746 blood
14 chr7:17672400-17673400 Enhancers NHDF-Ad bronchial
15 chr7:17672600-17673000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr7:17672600-17673000 Enhancers Duodenum Mucosa Duodenum
17 chr7:17672600-17673000 Flanking Active TSS A549 lung
18 chr7:17672600-17673200 Enhancers Fetal Adrenal Gland Adrenal Gland
19 chr7:17672600-17673400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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