Variant report

Variant rs55885267
Chromosome Location chr9:139652017-139652018
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139648000-139658200 Enhancers Primary B cells from peripheral blood blood
2 chr9:139649600-139654800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr9:139650000-139655200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr9:139650600-139652800 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:139651000-139656200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr9:139651200-139653000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr9:139651400-139657400 Weak transcription Right Atrium heart
8 chr9:139651600-139653800 Enhancers Fetal Muscle Leg muscle
9 chr9:139651800-139652200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:139651800-139652200 Enhancers Fetal Muscle Trunk muscle
11 chr9:139651800-139652800 Enhancers Psoas Muscle Psoas
12 chr9:139651800-139653000 Flanking Active TSS Skeletal Muscle Male skeletal muscle
13 chr9:139652000-139652200 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr9:139652000-139652400 Active TSS Skeletal Muscle Female skeletal muscle
15 chr9:139652000-139653000 Bivalent Enhancer Muscle Satellite Cultured Cells --
16 chr9:139652000-139653000 Enhancers HSMMtube muscle
17 chr9:139652000-139655800 Enhancers Primary B cells from cord blood blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links