Variant report

Variant rs11991779
Chromosome Location chr8:49626240-49626241
allele A/C
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 chr8:49621600-49628600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr8:49622400-49628000 Weak transcription Ovary ovary
5 chr8:49622800-49627400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr8:49622800-49627600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr8:49624200-49627000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr8:49624400-49627000 Enhancers HMEC breast
9 chr8:49624400-49627200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr8:49625600-49627000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr8:49625800-49626800 Enhancers Placenta Placenta
12 chr8:49626000-49626400 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr8:49626000-49626400 Enhancers Fetal Kidney kidney
14 chr8:49626000-49626600 Weak transcription Esophagus oesophagus
15 chr8:49626000-49626800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr8:49626200-49626400 Enhancers Spleen Spleen
17 chr8:49626200-49626600 Enhancers NHEK skin
18 chr8:49626200-49627400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

Quick Search:


  
Input of quick search could be:

what's new

Quick links