Variant report

Variant rs10101066
Chromosome Location chr8:49626192-49626193
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49612800-49626400 Weak transcription Placenta Amnion Placenta Amnion
2 chr8:49618200-49628000 Weak transcription Fetal Lung lung
3 chr8:49619000-49626200 Weak transcription Spleen Spleen
4 chr8:49621600-49628600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr8:49622400-49628000 Weak transcription Ovary ovary
6 chr8:49622800-49627400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr8:49622800-49627600 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr8:49624200-49627000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr8:49624400-49627000 Enhancers HMEC breast
10 chr8:49624400-49627200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr8:49625600-49627000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr8:49625800-49626200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr8:49625800-49626800 Enhancers Placenta Placenta
14 chr8:49626000-49626200 Flanking Active TSS NHEK skin
15 chr8:49626000-49626400 Enhancers Fetal Adrenal Gland Adrenal Gland
16 chr8:49626000-49626400 Enhancers Fetal Kidney kidney
17 chr8:49626000-49626600 Weak transcription Esophagus oesophagus
18 chr8:49626000-49626800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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