Variant report

Variant rs6841224
Chromosome Location chr4:189117032-189117033
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:189105200-189117400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:189116600-189117200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr4:189116600-189117200 Enhancers Brain Substantia Nigra brain
4 chr4:189116600-189117200 Enhancers Fetal Muscle Leg muscle
5 chr4:189116600-189117600 Enhancers Fetal Lung lung
6 chr4:189116800-189117200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr4:189116800-189117200 Enhancers Brain Hippocampus Middle brain
8 chr4:189116800-189117200 Enhancers Fetal Heart heart
9 chr4:189116800-189117200 Enhancers Osteobl bone
10 chr4:189116800-189117400 Enhancers Brain Cingulate Gyrus brain
11 chr4:189116800-189117400 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr4:189116800-189118000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr4:189117000-189117200 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:189117000-189117400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
15 chr4:189117000-189117600 Enhancers HUES64 Cell Line embryonic stem cell
16 chr4:189117000-189117600 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr4:189117000-189117600 Active TSS Aorta Aorta
18 chr4:189117000-189117800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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