Variant report

Variant rs13107539
Chromosome Location chr4:188049114-188049115
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:188045800-188050200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:188047400-188049600 Weak transcription HSMMtube muscle
3 chr4:188048200-188049600 Enhancers HMEC breast
4 chr4:188048400-188049600 Enhancers Muscle Satellite Cultured Cells --
5 chr4:188048400-188049600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr4:188048400-188049600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr4:188048400-188049600 Enhancers NHEK skin
8 chr4:188048600-188049400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr4:188048600-188049600 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr4:188048600-188049600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:188048600-188049600 Enhancers NH-A brain
12 chr4:188048800-188049800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr4:188049000-188049400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr4:188049000-188049400 Weak transcription HSMM muscle

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