Variant report

Variant rs9261111
Chromosome Location chr6:29976499-29976500
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29974800-29981000 Weak transcription Hela-S3 cervix
2 chr6:29974800-30002400 Weak transcription Dnd41 blood
3 chr6:29975200-29976600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:29975200-30027800 Weak transcription Aorta Aorta
5 chr6:29975400-29978800 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr6:29975400-29985200 Weak transcription Lung lung
7 chr6:29975600-29979200 Weak transcription Ovary ovary
8 chr6:29975600-29979200 Weak transcription Pancreas Pancrea
9 chr6:29975600-29985000 Weak transcription Liver Liver
10 chr6:29975600-29985200 Weak transcription Primary B cells from cord blood blood
11 chr6:29975600-29987200 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr6:29975600-29987600 Weak transcription HepG2 liver
13 chr6:29975600-30027800 Weak transcription Right Ventricle heart
14 chr6:29975800-29986600 Weak transcription Esophagus oesophagus
15 chr6:29975800-30027800 Weak transcription Gastric stomach
16 chr6:29976200-29986600 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
17 chr6:29976200-29987800 Weak transcription Primary B cells from peripheral blood blood
18 chr6:29976200-30001800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr6:29976400-29977800 Strong transcription Spleen Spleen

Quick Search:


  
Input of quick search could be:

what's new

Quick links