Variant report

Variant rs9773582
Chromosome Location chr8:49668964-49668965
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49663600-49669600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:49664400-49669000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr8:49664800-49669400 Weak transcription Spleen Spleen
4 chr8:49665600-49669400 Weak transcription Lung lung
5 chr8:49666400-49669400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:49666400-49670000 Weak transcription Osteobl bone
7 chr8:49666400-49670200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:49666400-49670600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr8:49666600-49669200 Weak transcription HMEC breast
10 chr8:49666600-49669800 Weak transcription NHDF-Ad bronchial
11 chr8:49666600-49670000 Weak transcription Muscle Satellite Cultured Cells --
12 chr8:49666600-49670000 Weak transcription NHEK skin
13 chr8:49666800-49669400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr8:49666800-49671400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr8:49667200-49670000 Weak transcription Fetal Lung lung
16 chr8:49668200-49671400 Enhancers Pancreas Pancrea
17 chr8:49668400-49672000 Enhancers Breast Myoepithelial Primary Cells Breast
18 chr8:49668600-49670800 Enhancers Fetal Muscle Trunk muscle
19 chr8:49668800-49671400 Enhancers Ovary ovary

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