Variant report
Variant | rs72778028 |
---|---|
Chromosome Location | chr5:79589770-79589771 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10036141 | 1.00[ASN][1000 genomes] |
rs10036779 | 1.00[ASN][1000 genomes] |
rs10041410 | 1.00[ASN][1000 genomes] |
rs10058560 | 1.00[ASN][1000 genomes] |
rs10068511 | 1.00[ASN][1000 genomes] |
rs12697906 | 1.00[ASN][1000 genomes] |
rs13170471 | 1.00[ASN][1000 genomes] |
rs13178966 | 1.00[ASN][1000 genomes] |
rs13180605 | 1.00[ASN][1000 genomes] |
rs13186656 | 1.00[ASN][1000 genomes] |
rs13187742 | 1.00[ASN][1000 genomes] |
rs13355153 | 1.00[ASN][1000 genomes] |
rs17200856 | 1.00[ASN][1000 genomes] |
rs17201124 | 1.00[ASN][1000 genomes] |
rs2405138 | 1.00[ASN][1000 genomes] |
rs28637244 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35696683 | 1.00[ASN][1000 genomes] |
rs4521455 | 1.00[ASN][1000 genomes] |
rs56040222 | 1.00[ASN][1000 genomes] |
rs6867389 | 1.00[ASN][1000 genomes] |
rs6867803 | 1.00[ASN][1000 genomes] |
rs6876065 | 1.00[ASN][1000 genomes] |
rs6888220 | 1.00[ASN][1000 genomes] |
rs71636208 | 1.00[ASN][1000 genomes] |
rs72778006 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9293805 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948807 | chr5:79549207-79805765 | Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
2 | nsv518480 | chr5:79586085-79748382 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:79580600-79595400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |