Variant report

Variant rs57958042
Chromosome Location chr17:16906073-16906074
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16903200-16921000 Weak transcription Lung lung
2 chr17:16904600-16906400 Enhancers Liver Liver
3 chr17:16904600-16906600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr17:16904800-16906400 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr17:16904800-16906400 Enhancers A549 lung
6 chr17:16905200-16906200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr17:16905200-16906200 Enhancers Placenta Amnion Placenta Amnion
8 chr17:16905400-16906200 Enhancers Fetal Thymus thymus
9 chr17:16905400-16906400 Enhancers Fetal Muscle Leg muscle
10 chr17:16905400-16906800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr17:16905400-16907800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr17:16905600-16906200 Enhancers Brain Hippocampus Middle brain
13 chr17:16905600-16906600 Weak transcription Fetal Lung lung
14 chr17:16905600-16907600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr17:16905800-16906200 Weak transcription Skeletal Muscle Male skeletal muscle
16 chr17:16905800-16906400 Enhancers Brain Substantia Nigra brain
17 chr17:16905800-16920000 Weak transcription Fetal Intestine Large intestine
18 chr17:16906000-16906200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
19 chr17:16906000-16906800 Weak transcription H1 Cell Line embryonic stem cell

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