Variant report

Variant rs4554144
Chromosome Location chr4:69960555-69960556
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69958000-69960800 Weak transcription HUVEC blood vessel
2 chr4:69958200-69961000 Weak transcription HMEC breast
3 chr4:69958400-69961800 Weak transcription Osteobl bone
4 chr4:69959200-69961000 Enhancers A549 lung
5 chr4:69959400-69960800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr4:69959600-69960800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr4:69959600-69960800 Weak transcription Fetal Intestine Small intestine
8 chr4:69959600-69960800 Weak transcription NH-A brain
9 chr4:69959600-69980000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr4:69960000-69962000 Enhancers HepG2 liver
11 chr4:69960200-69962600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr4:69960400-69960600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr4:69960400-69960800 Enhancers Muscle Satellite Cultured Cells --
14 chr4:69960400-69962200 Enhancers Fetal Intestine Large intestine
15 chr4:69960400-69962400 Enhancers NHEK skin

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