Variant report

Variant rs73362232
Chromosome Location chr14:104673952-104673953
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104672000-104674000 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
2 chr14:104672200-104674000 Enhancers Fetal Intestine Small intestine
3 chr14:104672200-104674400 Enhancers Brain Germinal Matrix brain
4 chr14:104672400-104674000 Enhancers Cortex derived primary cultured neurospheres brain
5 chr14:104672400-104674200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr14:104672400-104674200 Enhancers Fetal Brain Male brain
7 chr14:104673000-104674400 Enhancers Spleen Spleen
8 chr14:104673200-104674200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
9 chr14:104673200-104676600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr14:104673200-104676600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
11 chr14:104673400-104676800 Weak transcription Brain Cingulate Gyrus brain
12 chr14:104673800-104674000 Enhancers Fetal Brain Female brain
13 chr14:104673800-104675400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr14:104673800-104677000 Weak transcription Fetal Lung lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links