Variant report

Variant rs9886604
Chromosome Location chr8:49747888-49747889
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49734000-49748200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:49746200-49751000 Weak transcription Fetal Kidney kidney
3 chr8:49746600-49748000 Weak transcription Fetal Lung lung
4 chr8:49746600-49748600 Enhancers Fetal Muscle Trunk muscle
5 chr8:49746800-49751000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr8:49746800-49751600 Weak transcription Pancreas Pancrea
7 chr8:49747000-49748000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr8:49747400-49748000 Enhancers Esophagus oesophagus
9 chr8:49747400-49748600 Enhancers Spleen Spleen
10 chr8:49747600-49748000 Enhancers Brain Germinal Matrix brain
11 chr8:49747600-49748600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr8:49747600-49748600 Enhancers Fetal Muscle Leg muscle
13 chr8:49747600-49748600 Bivalent Enhancer Fetal Stomach stomach
14 chr8:49747600-49748800 Enhancers Placenta Amnion Placenta Amnion
15 chr8:49747800-49748400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr8:49747800-49748400 Enhancers NHEK skin
17 chr8:49747800-49748600 Enhancers Fetal Adrenal Gland Adrenal Gland
18 chr8:49747800-49748800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr8:49747800-49748800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr8:49747800-49749400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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