Variant report
Variant | rs1241197 |
---|---|
Chromosome Location | chr1:103310111-103310112 |
allele | G/T |
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] |
---|---|
rs1031820 | 0.80[AMR][1000 genomes] |
rs1241172 | 0.95[ASN][1000 genomes] |
rs1241173 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs1241190 | 1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs12748410 | 0.90[ASN][1000 genomes] |
rs12749981 | 0.95[ASN][1000 genomes] |
rs12752702 | 0.90[ASN][1000 genomes] |
rs1676491 | 0.80[AMR][1000 genomes] |
rs1763350 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs1932336 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs1932342 | 0.92[ASN][1000 genomes] |
rs2598461 | 0.92[ASN][1000 genomes] |
rs2615999 | 0.80[AMR][1000 genomes] |
rs2708397 | 0.92[ASN][1000 genomes] |
rs474472 | 0.92[ASN][1000 genomes] |
rs511308 | 0.92[ASN][1000 genomes] |
rs514077 | 0.92[ASN][1000 genomes] |
rs579692 | 0.90[ASN][1000 genomes] |
rs583527 | 0.92[ASN][1000 genomes] |
rs606756 | 0.92[ASN][1000 genomes] |
rs618072 | 0.92[ASN][1000 genomes] |
rs621734 | 0.92[ASN][1000 genomes] |
rs629282 | 0.92[ASN][1000 genomes] |
rs631137 | 0.92[ASN][1000 genomes] |
rs636801 | 0.90[ASN][1000 genomes] |
rs670939 | 0.92[ASN][1000 genomes] |
rs72681287 | 0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830882 | chr1:103192683-103355802 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv522922 | chr1:103305021-103764640 | Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:103308600-103310800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |