Variant report

Variant rs1080267
Chromosome Location chr1:169176469-169176470
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169130400-169195200 Weak transcription Pancreas Pancrea
2 chr1:169163600-169184000 Weak transcription Ovary ovary
3 chr1:169167800-169186800 Weak transcription Primary T cells from cord blood blood
4 chr1:169168000-169183800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr1:169171600-169184000 Weak transcription Fetal Intestine Small intestine
6 chr1:169172000-169176600 Weak transcription Colon Smooth Muscle Colon
7 chr1:169172400-169183800 Weak transcription Brain Germinal Matrix brain
8 chr1:169172400-169207600 Weak transcription Esophagus oesophagus
9 chr1:169172600-169227000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:169173200-169202000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr1:169173600-169183800 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr1:169176400-169176600 Enhancers Aorta Aorta
13 chr1:169176400-169177000 Enhancers Rectal Smooth Muscle rectum
14 chr1:169176400-169177800 Enhancers Breast Myoepithelial Primary Cells Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links