Variant report

Variant rs73594165
Chromosome Location chr6:143581829-143581830
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143545400-143588800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:143564200-143583000 Weak transcription Pancreas Pancrea
3 chr6:143569000-143592000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr6:143569200-143586600 Weak transcription Stomach Smooth Muscle stomach
5 chr6:143569600-143588600 Weak transcription Aorta Aorta
6 chr6:143570800-143609200 Weak transcription Fetal Intestine Large intestine
7 chr6:143574400-143583000 Weak transcription Liver Liver
8 chr6:143576200-143585800 Weak transcription Fetal Lung lung
9 chr6:143579000-143585600 Weak transcription Fetal Stomach stomach
10 chr6:143579800-143589400 Weak transcription Left Ventricle heart
11 chr6:143581000-143585600 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr6:143581600-143582200 Enhancers NHEK skin
13 chr6:143581600-143582400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr6:143581600-143582600 Enhancers HMEC breast
15 chr6:143581800-143582200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr6:143581800-143582200 Enhancers NHDF-Ad bronchial
17 chr6:143581800-143582200 Enhancers Osteobl bone
18 chr6:143581800-143582400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr6:143581800-143582400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
20 chr6:143581800-143582400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
21 chr6:143581800-143582600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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