Variant report
Variant | rs72748633 |
---|---|
Chromosome Location | chr5:42014597-42014598 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:42010842..42015595-chr5:42016092..42019954,4 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10044526 | 1.00[EUR][1000 genomes] |
rs11738449 | 1.00[EUR][1000 genomes] |
rs11738956 | 0.86[AMR][1000 genomes] |
rs11742939 | 1.00[EUR][1000 genomes] |
rs11744111 | 0.81[EUR][1000 genomes] |
rs13360765 | 0.98[EUR][1000 genomes] |
rs16872094 | 1.00[EUR][1000 genomes] |
rs16872097 | 1.00[EUR][1000 genomes] |
rs16872099 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16872100 | 0.96[EUR][1000 genomes] |
rs16872111 | 0.96[EUR][1000 genomes] |
rs16872114 | 1.00[EUR][1000 genomes] |
rs1813615 | 1.00[EUR][1000 genomes] |
rs1813616 | 1.00[EUR][1000 genomes] |
rs2011105 | 1.00[EUR][1000 genomes] |
rs2113053 | 0.91[EUR][1000 genomes] |
rs2161581 | 1.00[EUR][1000 genomes] |
rs4626371 | 0.81[EUR][1000 genomes] |
rs4957182 | 0.89[EUR][1000 genomes] |
rs59778370 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs666581 | 0.81[EUR][1000 genomes] |
rs6870241 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72746930 | 0.90[AMR][1000 genomes] |
rs72746933 | 0.90[AMR][1000 genomes] |
rs72746952 | 0.90[AMR][1000 genomes] |
rs72746962 | 0.90[AMR][1000 genomes] |
rs72746968 | 0.90[AMR][1000 genomes] |
rs72746975 | 0.90[AMR][1000 genomes] |
rs72746995 | 0.81[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs72747001 | 0.81[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs72748623 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs72748626 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs72748630 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs72748631 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs72748635 | 1.00[EUR][1000 genomes] |
rs72748636 | 1.00[EUR][1000 genomes] |
rs72748638 | 1.00[EUR][1000 genomes] |
rs72748639 | 1.00[EUR][1000 genomes] |
rs72748641 | 1.00[EUR][1000 genomes] |
rs72748645 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs72748646 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72748687 | 0.81[EUR][1000 genomes] |
rs72748699 | 0.81[EUR][1000 genomes] |
rs989747 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830273 | chr5:41867296-42066070 | Flanking Active TSS Active TSS Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 111 gene(s) | inside rSNPs | diseases |
2 | nsv933208 | chr5:41879946-42876624 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 112 gene(s) | inside rSNPs | diseases |
3 | nsv492147 | chr5:41902086-42896162 | Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 113 gene(s) | inside rSNPs | diseases |
4 | nsv880627 | chr5:41966551-42087954 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
5 | esv1843569 | chr5:42008999-42128184 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:42013400-42015600 | Enhancers | Liver | Liver |
2 | chr5:42014400-42016400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |