Variant report

Variant rs10135121
Chromosome Location chr14:104891816-104891817
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104886200-104892800 Enhancers Fetal Brain Male brain
2 chr14:104886600-104894200 Enhancers Brain Germinal Matrix brain
3 chr14:104886800-104892600 Enhancers Fetal Brain Female brain
4 chr14:104887200-104893200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr14:104887400-104892600 Bivalent Enhancer Fetal Muscle Leg muscle
6 chr14:104887400-104892800 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr14:104888400-104892000 Bivalent Enhancer Fetal Stomach stomach
8 chr14:104888800-104902400 Weak transcription Right Atrium heart
9 chr14:104889400-104892400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr14:104890200-104892400 Enhancers Ovary ovary
11 chr14:104890600-104892400 Enhancers Fetal Heart heart
12 chr14:104890800-104892000 Enhancers Brain Cingulate Gyrus brain
13 chr14:104891000-104892200 Enhancers H1 Cell Line embryonic stem cell
14 chr14:104891200-104892600 Enhancers Spleen Spleen
15 chr14:104891400-104892000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr14:104891800-104902200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links