Variant report

Variant rs73584929
Chromosome Location chr11:121066420-121066421
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121058800-121069000 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr11:121062600-121070000 Weak transcription Fetal Heart heart
3 chr11:121064600-121069000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:121065800-121070200 Weak transcription H9 Cell Line embryonic stem cell
5 chr11:121066000-121067600 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr11:121066000-121068800 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr11:121066000-121068800 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr11:121066000-121068800 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr11:121066000-121069200 Weak transcription H1 Cell Line embryonic stem cell
10 chr11:121066400-121069200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr11:121066400-121069200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links