Variant report

Variant rs55953601
Chromosome Location chr6:134431122-134431123
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:134416200-134438600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:134430200-134431200 Enhancers A549 lung
3 chr6:134430200-134432000 Enhancers Monocytes-CD14+_RO01746 blood
4 chr6:134430400-134431400 Enhancers Muscle Satellite Cultured Cells --
5 chr6:134430400-134432000 Enhancers Primary monocytes fromperipheralblood blood
6 chr6:134430400-134432000 Enhancers Hela-S3 cervix
7 chr6:134430600-134431400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr6:134430600-134431400 Enhancers Primary neutrophils fromperipheralblood blood
9 chr6:134430600-134431400 Enhancers Placenta Placenta
10 chr6:134430800-134431400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr6:134430800-134431400 Enhancers HMEC breast
12 chr6:134430800-134431400 Enhancers Osteobl bone
13 chr6:134431000-134431200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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