Variant report

Variant rs863720
Chromosome Location chr1:180296781-180296782
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180278000-180298200 Weak transcription Esophagus oesophagus
2 chr1:180279000-180297600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr1:180279600-180298800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:180281000-180329400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:180282800-180313400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:180283000-180302800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr1:180283000-180302800 Weak transcription Fetal Intestine Large intestine
8 chr1:180294400-180303000 Weak transcription Placenta Placenta
9 chr1:180295600-180297000 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr1:180295800-180302600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:180295800-180309200 Weak transcription Primary B cells from cord blood blood
12 chr1:180296000-180297600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr1:180296000-180298000 Weak transcription Fetal Stomach stomach
14 chr1:180296200-180298200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:180296200-180302600 Weak transcription Pancreas Pancrea
16 chr1:180296400-180302400 Weak transcription Dnd41 blood
17 chr1:180296600-180301200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr1:180296600-180302600 Weak transcription Primary hematopoietic stem cells short term culture blood
19 chr1:180296600-180309000 Weak transcription Primary T cells from cord blood blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links