UCSC Genome Browser on Human Dec. 2013 (GRCh38/hg38) Assembly
move zoom in zoom out
chr1:10,467,863-10,467,869 7 bp.
move start
  Click on a feature for details. Click+shift+drag to zoom in. Click side bars for track options. Drag side bars or labels up or down to reorder tracks. Drag tracks left or right to new position. Press "?" for keyboard shortcuts.   move end
  
Use drop-down controls below and press refresh to alter tracks displayed.
Tracks with lots of items will automatically be displayed in more compact modes.
-   Mapping and Sequencing
Base Position
p12 Assembly
p12 Chromosome Band
p12 Gap
Short Match
-   Genes and Gene Predictions
NCBI RefSeq
Ribo-seq SmProt ATG
Ribo-seq SmProt nonATG
literature SmProt
database SmProt
MS SmProt
NONCODE
p12 All GENCODE...
-   Phenotype and Literature
ClinVar Variants
-   Comparative Genomics
Conservation
-   Variation
Common SNPs(150)
All SNPs(150)
Flagged SNPs(150)
Mult. SNPs(150)
smprot variants
gnomAD Variants...
NyuWa variants
-   Repeats
p12 RepeatMasker