Variant report
Variant | rs1361124 |
---|---|
Chromosome Location | chr1:94816865-94816866 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000117528 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10399782 | 1.00[EUR][1000 genomes] |
rs10782981 | 1.00[EUR][1000 genomes] |
rs10874845 | 1.00[EUR][1000 genomes] |
rs1146478 | 1.00[EUR][1000 genomes] |
rs1146479 | 1.00[EUR][1000 genomes] |
rs1146506 | 1.00[EUR][1000 genomes] |
rs1146516 | 1.00[EUR][1000 genomes] |
rs11801203 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11801251 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11805161 | 1.00[EUR][1000 genomes] |
rs11810728 | 0.83[AFR][1000 genomes] |
rs12069536 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1303136 | 1.00[EUR][1000 genomes] |
rs1318396 | 1.00[EUR][1000 genomes] |
rs1330856 | 1.00[EUR][1000 genomes] |
rs1330858 | 1.00[EUR][1000 genomes] |
rs1330859 | 1.00[EUR][1000 genomes] |
rs1330860 | 1.00[EUR][1000 genomes] |
rs1337856 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1337857 | 1.00[EUR][1000 genomes] |
rs1411697 | 1.00[EUR][1000 genomes] |
rs1411703 | 1.00[EUR][1000 genomes] |
rs1571645 | 1.00[EUR][1000 genomes] |
rs1577920 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1616972 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1617363 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1617719 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687921 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687922 | 1.00[EUR][1000 genomes] |
rs1687923 | 1.00[EUR][1000 genomes] |
rs1687925 | 1.00[EUR][1000 genomes] |
rs1687926 | 1.00[EUR][1000 genomes] |
rs1687929 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687934 | 1.00[EUR][1000 genomes] |
rs1687938 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687939 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687942 | 1.00[EUR][1000 genomes] |
rs1687945 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687953 | 0.96[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687955 | 1.00[EUR][1000 genomes] |
rs1687958 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687959 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687960 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1687967 | 1.00[EUR][1000 genomes] |
rs1687969 | 1.00[EUR][1000 genomes] |
rs17111347 | 1.00[EUR][1000 genomes] |
rs1749540 | 1.00[EUR][1000 genomes] |
rs1756247 | 1.00[EUR][1000 genomes] |
rs1756256 | 1.00[EUR][1000 genomes] |
rs1756258 | 1.00[EUR][1000 genomes] |
rs1756263 | 1.00[EUR][1000 genomes] |
rs1756264 | 1.00[EUR][1000 genomes] |
rs1765616 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765624 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765625 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765631 | 0.84[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765633 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765634 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765637 | 0.81[AFR][1000 genomes] |
rs1765638 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765639 | 1.00[EUR][1000 genomes] |
rs1765642 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1765653 | 1.00[EUR][1000 genomes] |
rs2021993 | 1.00[EUR][1000 genomes] |
rs2094824 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs2391471 | 1.00[EUR][1000 genomes] |
rs2483792 | 1.00[EUR][1000 genomes] |
rs2774921 | 1.00[EUR][1000 genomes] |
rs2798944 | 1.00[EUR][1000 genomes] |
rs28494821 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs2893296 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2971948 | 1.00[EUR][1000 genomes] |
rs479627 | 1.00[EUR][1000 genomes] |
rs484420 | 1.00[EUR][1000 genomes] |
rs4847297 | 1.00[EUR][1000 genomes] |
rs512648 | 1.00[EUR][1000 genomes] |
rs513976 | 1.00[EUR][1000 genomes] |
rs529642 | 1.00[EUR][1000 genomes] |
rs598962 | 1.00[EUR][1000 genomes] |
rs610088 | 1.00[EUR][1000 genomes] |
rs630382 | 1.00[EUR][1000 genomes] |
rs6660037 | 1.00[EUR][1000 genomes] |
rs6684237 | 1.00[EUR][1000 genomes] |
rs698945 | 1.00[EUR][1000 genomes] |
rs7417304 | 1.00[EUR][1000 genomes] |
rs7548077 | 1.00[EUR][1000 genomes] |
rs768967 | 1.00[EUR][1000 genomes] |
rs860909 | 1.00[EUR][1000 genomes] |
rs9432270 | 1.00[EUR][1000 genomes] |
rs9432441 | 1.00[EUR][1000 genomes] |
rs9432688 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428510 | chr1:94709575-94866655 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:94814400-94821400 | Enhancers | Fetal Thymus | thymus |
2 | chr1:94814600-94819000 | Enhancers | Thymus | Thymus |
3 | chr1:94815000-94818000 | Enhancers | HepG2 | liver |
4 | chr1:94816400-94818000 | Enhancers | Dnd41 | blood |
5 | chr1:94816800-94817800 | Enhancers | Placenta | Placenta |
6 | chr1:94816800-94820400 | Weak transcription | Liver | Liver |