Variant report

Variant rs151096049
Chromosome Location chr4:1395911-1395912
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1391200-1396600 Weak transcription Right Atrium heart
2 chr4:1393200-1397000 Weak transcription Gastric stomach
3 chr4:1394800-1397400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr4:1395400-1396800 Bivalent Enhancer Primary B cells from peripheral blood blood
5 chr4:1395600-1396200 Bivalent Enhancer Primary B cells from cord blood blood
6 chr4:1395600-1396200 Bivalent Enhancer Spleen Spleen
7 chr4:1395600-1396600 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
8 chr4:1395600-1398000 Bivalent Enhancer Esophagus oesophagus
9 chr4:1395800-1396000 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
10 chr4:1395800-1396000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
11 chr4:1395800-1397400 Bivalent Enhancer Primary hematopoietic stem cells blood
12 chr4:1395800-1397400 Bivalent Enhancer Primary T cells effector/memory enriched fromperipheralblood blood
13 chr4:1395800-1399200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr4:1395800-1399400 Bivalent Enhancer Fetal Muscle Trunk muscle

Quick Search:


  
Input of quick search could be:

what's new

Quick links