Variant report

Variant rs4288587
Chromosome Location chr1:154492357-154492358
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:154488600-154497400 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr1:154491800-154493000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:154491800-154493000 Enhancers NHEK skin
4 chr1:154491800-154493200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:154492000-154492600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr1:154492000-154492600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:154492000-154492600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:154492000-154492600 Enhancers Fetal Heart heart
9 chr1:154492000-154492600 Flanking Active TSS Hela-S3 cervix
10 chr1:154492000-154493800 Enhancers Left Ventricle heart
11 chr1:154492000-154493800 Enhancers Right Atrium heart
12 chr1:154492000-154494000 Enhancers Placenta Placenta
13 chr1:154492000-154494800 Enhancers Adipose Nuclei Adipose
14 chr1:154492000-154494800 Enhancers Right Ventricle heart
15 chr1:154492000-154495200 Enhancers Lung lung
16 chr1:154492200-154492400 Enhancers Esophagus oesophagus
17 chr1:154492200-154492600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr1:154492200-154494000 Enhancers Spleen Spleen

Quick Search:


  
Input of quick search could be:

what's new

Quick links