Variant report

Variant rs4721636
Chromosome Location chr7:17648006-17648007
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17641600-17663000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:17642400-17657400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr7:17646200-17648800 Enhancers Hela-S3 cervix
4 chr7:17646600-17648800 Enhancers NHDF-Ad bronchial
5 chr7:17647400-17648600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr7:17647400-17648600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:17647400-17648800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr7:17647400-17648800 Enhancers Muscle Satellite Cultured Cells --
9 chr7:17647400-17648800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr7:17647400-17648800 Enhancers HSMM muscle
11 chr7:17647400-17649200 Enhancers Monocytes-CD14+_RO01746 blood
12 chr7:17647600-17648400 Enhancers Primary monocytes fromperipheralblood blood
13 chr7:17647600-17648600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr7:17647600-17648600 Enhancers HMEC breast
15 chr7:17647600-17648600 Enhancers Osteobl bone
16 chr7:17647600-17648800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr7:17647600-17648800 Enhancers HSMMtube muscle
18 chr7:17647600-17648800 Enhancers NHLF lung
19 chr7:17648000-17648600 Enhancers Fetal Intestine Large intestine

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