Variant report
Variant | rs74102908 |
---|---|
Chromosome Location | chr13:85094688-85094689 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-SLITRK5-32 | chr13:85094238-85095703 | NONHSAT034551 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs3887000 | 1.00[EUR][1000 genomes] |
rs55952775 | 0.94[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs56117650 | 1.00[EUR][1000 genomes] |
rs56707798 | 1.00[EUR][1000 genomes] |
rs59655414 | 1.00[EUR][1000 genomes] |
rs59995957 | 1.00[EUR][1000 genomes] |
rs74102909 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74102934 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74102935 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74102938 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74102945 | 1.00[EUR][1000 genomes] |
rs74102947 | 1.00[EUR][1000 genomes] |
rs7998340 | 1.00[EUR][1000 genomes] |
rs7998673 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7999286 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs8001368 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs8002485 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949402 | chr13:84675752-85606846 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv456046 | chr13:84971270-85262508 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv562561 | chr13:84971270-85262508 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv832666 | chr13:85028182-85193796 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1054691 | chr13:85078280-85100978 | Enhancers | TF binding regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |