Variant report
Variant | rs7714784 |
---|---|
Chromosome Location | chr5:128155249-128155250 |
allele | A/G |
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] |
---|---|
rs10058979 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10058982 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1035407 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10520015 | 0.89[ASN][1000 genomes] |
rs1118881 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1345608 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1421887 | 0.90[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs1422443 | 0.80[EUR][1000 genomes] |
rs1603409 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1988891 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2012809 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2079100 | 0.86[ASN][1000 genomes] |
rs2106977 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2310809 | 0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2522379 | 0.89[ASN][1000 genomes] |
rs2522380 | 0.89[ASN][1000 genomes] |
rs2522382 | 0.89[ASN][1000 genomes] |
rs2522384 | 0.89[ASN][1000 genomes] |
rs2522386 | 0.89[ASN][1000 genomes] |
rs2545018 | 0.89[ASN][1000 genomes] |
rs2545019 | 0.89[ASN][1000 genomes] |
rs2545020 | 0.89[ASN][1000 genomes] |
rs2545021 | 0.90[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs2545023 | 0.90[AFR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2577464 | 0.89[ASN][1000 genomes] |
rs2577466 | 0.89[ASN][1000 genomes] |
rs2577467 | 0.89[ASN][1000 genomes] |
rs2577469 | 0.90[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs34217034 | 0.89[ASN][1000 genomes] |
rs55721000 | 0.89[ASN][1000 genomes] |
rs55729238 | 0.89[ASN][1000 genomes] |
rs55745082 | 0.89[ASN][1000 genomes] |
rs55936379 | 0.89[ASN][1000 genomes] |
rs56105026 | 0.86[ASN][1000 genomes] |
rs56285759 | 0.86[ASN][1000 genomes] |
rs6897985 | 0.90[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs72795284 | 0.89[ASN][1000 genomes] |
rs72795288 | 0.89[ASN][1000 genomes] |
rs72795289 | 0.89[ASN][1000 genomes] |
rs72795290 | 0.89[ASN][1000 genomes] |
rs72795292 | 0.89[ASN][1000 genomes] |
rs72795293 | 0.89[ASN][1000 genomes] |
rs72795295 | 0.89[ASN][1000 genomes] |
rs72795296 | 0.89[ASN][1000 genomes] |
rs72795297 | 0.89[ASN][1000 genomes] |
rs72795300 | 0.89[ASN][1000 genomes] |
rs72795301 | 0.89[ASN][1000 genomes] |
rs72795302 | 0.89[ASN][1000 genomes] |
rs72797158 | 0.89[ASN][1000 genomes] |
rs72797159 | 0.89[ASN][1000 genomes] |
rs72797161 | 0.89[ASN][1000 genomes] |
rs72797166 | 0.89[ASN][1000 genomes] |
rs72797172 | 0.88[ASN][1000 genomes] |
rs72797173 | 0.89[ASN][1000 genomes] |
rs72797175 | 0.89[ASN][1000 genomes] |
rs72797176 | 0.89[ASN][1000 genomes] |
rs72797178 | 0.89[ASN][1000 genomes] |
rs72797183 | 0.88[ASN][1000 genomes] |
rs72797186 | 0.89[ASN][1000 genomes] |
rs7700634 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7701236 | 0.89[ASN][1000 genomes] |
rs7719508 | 0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023405 | chr5:127955360-128190069 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | esv3392548 | chr5:128139102-128159002 | Enhancers Weak transcription Strong transcription ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:128151200-128157400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |