Variant report

Variant rs7664855
Chromosome Location chr4:53925571-53925572
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:53904800-53929800 Weak transcription Primary T cells from cord blood blood
2 chr4:53909000-53929400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr4:53921600-53933200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr4:53922000-53933600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr4:53922200-53945600 Weak transcription Ovary ovary
6 chr4:53922200-53954600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr4:53922600-53931400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr4:53922600-53933400 Weak transcription Osteobl bone
9 chr4:53924000-53925600 Enhancers Psoas Muscle Psoas
10 chr4:53924000-53925800 Enhancers Skeletal Muscle Female skeletal muscle
11 chr4:53924000-53926600 Enhancers Aorta Aorta
12 chr4:53924200-53932000 Weak transcription HepG2 liver
13 chr4:53924800-53925600 Enhancers Skeletal Muscle Male skeletal muscle
14 chr4:53925000-53925600 Enhancers Fetal Muscle Leg muscle
15 chr4:53925000-53925600 Enhancers Right Ventricle heart
16 chr4:53925400-53925800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr4:53925400-53925800 Enhancers Adipose Nuclei Adipose
18 chr4:53925400-53925800 Enhancers Stomach Smooth Muscle stomach
19 chr4:53925400-53926400 Weak transcription GM12878-XiMat blood

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