Variant report

Variant rs4871400
Chromosome Location chr8:124652313-124652314
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:124646000-124655800 Weak transcription Osteobl bone
2 chr8:124648000-124652600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr8:124648800-124656000 Weak transcription Brain Hippocampus Middle brain
4 chr8:124650200-124655600 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr8:124650800-124652400 Enhancers Skeletal Muscle Male skeletal muscle
6 chr8:124650800-124652400 Enhancers Skeletal Muscle Female skeletal muscle
7 chr8:124651400-124653600 Enhancers Ovary ovary
8 chr8:124651600-124653200 Enhancers Right Atrium heart
9 chr8:124651800-124652400 Enhancers Stomach Smooth Muscle stomach
10 chr8:124651800-124653000 Enhancers Aorta Aorta
11 chr8:124651800-124653000 Enhancers Right Ventricle heart
12 chr8:124651800-124653200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr8:124651800-124653200 Enhancers Psoas Muscle Psoas
14 chr8:124651800-124653600 Enhancers Colon Smooth Muscle Colon
15 chr8:124651800-124653600 Enhancers Fetal Heart heart
16 chr8:124651800-124653600 Enhancers Left Ventricle heart
17 chr8:124652000-124653000 Enhancers Fetal Stomach stomach
18 chr8:124652000-124655800 Weak transcription Fetal Intestine Small intestine
19 chr8:124652200-124653200 Enhancers Fetal Muscle Trunk muscle
20 chr8:124652200-124653600 Enhancers Breast Myoepithelial Primary Cells Breast
21 chr8:124652200-124657800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
22 chr8:124652200-124658200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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