Variant report

Variant rs13274039
Chromosome Location chr8:8111659-8111660
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8106200-8113200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr8:8109200-8111800 Weak transcription Fetal Intestine Large intestine
3 chr8:8109200-8113000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:8109200-8113000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr8:8109600-8112200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr8:8109600-8112800 Weak transcription NHEK skin
7 chr8:8109600-8113000 Weak transcription HMEC breast
8 chr8:8109800-8119800 Weak transcription Fetal Lung lung
9 chr8:8110000-8112200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr8:8110200-8112800 Enhancers Placenta Amnion Placenta Amnion
11 chr8:8110600-8115000 Weak transcription Hela-S3 cervix
12 chr8:8111400-8112000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr8:8111400-8112200 Enhancers Liver Liver
14 chr8:8111400-8112400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr8:8111400-8112400 Enhancers Fetal Intestine Small intestine
16 chr8:8111600-8112000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr8:8111600-8112200 Flanking Active TSS HepG2 liver

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