Variant report

Variant rs6968786
Chromosome Location chr7:121942847-121942848
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:121939600-121943000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
2 chr7:121939800-121947600 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
3 chr7:121940000-121951000 Active TSS H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr7:121941200-121943400 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
5 chr7:121941200-121944400 Bivalent/Poised TSS hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr7:121942200-121943800 Weak transcription Right Atrium heart
7 chr7:121942400-121943000 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
8 chr7:121942600-121943000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
9 chr7:121942600-121943000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
10 chr7:121942600-121943000 Bivalent/Poised TSS ES-UCSF4 Cell Line embryonic stem cell
11 chr7:121942600-121944000 Bivalent/Poised TSS Brain Germinal Matrix brain
12 chr7:121942800-121943000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
13 chr7:121942800-121943200 Bivalent/Poised TSS H1 Cell Line embryonic stem cell
14 chr7:121942800-121944200 Active TSS Ganglion Eminence derived primary cultured neurospheres brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links