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Configure Tracks on UCSC Genome Browser: Human Dec. 2013 (GRCh38/hg38)
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-   Mapping and Sequencing    
Base Position Chromosome position in bases. (Clicks here zoom in 3x)
p12 Assembly Assembly from Fragments
p12 Chromosome Band Chromosome Bands Localized by FISH Mapping Clones
p12 Gap Gap Locations
Short Match Perfect Matches to Short Sequence ()
-   Genes and Gene Predictions    
NCBI RefSeq RefSeq gene predictions from NCBI
Ribo-seq SmProt ATG SmProt genes with ATG startcodon from Ribosome Profiling
Ribo-seq SmProt nonATG SmProt genes with non-ATG startcodon from Ribosome Profiling
literature SmProt SmProt genes from literature mining
database SmProt SmProt genes from other databases
MS SmProt SmProt genes from mass spectrum
NONCODE non-coding RNAs
p12 All GENCODE... All GENCODE transcripts, including comprehensive set and previous version
     All GENCODE V28     All GENCODE annotations from V28 (Ensembl 92)
-   Phenotype and Literature    
ClinVar Variants ClinVar Variants
-   Comparative Genomics    
Conservation Vertebrate Multiz Alignment & Conservation (100 Species)
-   Variation    
Common SNPs(150) Simple Nucleotide Polymorphisms (dbSNP 150) Found in >= 1% of Samples
All SNPs(150) Simple Nucleotide Polymorphisms (dbSNP 150)
Flagged SNPs(150) Simple Nucleotide Polymorphisms (dbSNP 150) Flagged by dbSNP as Clinically Assoc
Mult. SNPs(150) Simple Nucleotide Polymorphisms (dbSNP 150) That Map to Multiple Genomic Loci
smprot variants variants related to sORFs
gnomAD Variants... Genome Aggregation Database (gnomAD) Genome and Exome Variants
     gnomAD v3     Genome Aggregation Database (gnomAD) Genome Variants v3
NyuWa variants variants derived from NyuWa project
-   Repeats    
p12 RepeatMasker Repeating Elements by RepeatMasker