Variant report

Variant rs561075047
Chromosome Location chr4:74723387-74723388
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:74719400-74727800 Weak transcription NHLF lung
2 chr4:74719400-74733600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr4:74719600-74724800 Weak transcription Right Atrium heart
4 chr4:74719800-74723400 Weak transcription Pancreas Pancrea
5 chr4:74721400-74726000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr4:74721400-74729200 Weak transcription Primary neutrophils fromperipheralblood blood
7 chr4:74722200-74725000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr4:74722600-74724200 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr4:74722800-74723800 ZNF genes & repeats Muscle Satellite Cultured Cells --
10 chr4:74722800-74724800 Weak transcription Osteobl bone
11 chr4:74723000-74728000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:74723200-74723600 Enhancers Monocytes-CD14+_RO01746 blood
13 chr4:74723200-74723800 Enhancers Fetal Kidney kidney
14 chr4:74723200-74725200 Weak transcription Liver Liver

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