Variant report
Variant | rs2477285 |
---|---|
Chromosome Location | chr10:26964117-26964118 |
allele | C/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] |
---|---|
rs10764634 | 0.81[EUR][1000 genomes] |
rs1613801 | 0.81[EUR][1000 genomes] |
rs1616471 | 0.82[EUR][1000 genomes] |
rs1677711 | 0.84[EUR][1000 genomes] |
rs1677713 | 0.86[EUR][1000 genomes] |
rs1677714 | 0.86[EUR][1000 genomes] |
rs1677715 | 0.87[EUR][1000 genomes] |
rs1677727 | 0.82[EUR][1000 genomes] |
rs1677731 | 0.86[EUR][1000 genomes] |
rs1677732 | 0.83[EUR][1000 genomes] |
rs1677733 | 0.84[EUR][1000 genomes] |
rs1677734 | 0.84[EUR][1000 genomes] |
rs1677735 | 0.86[EUR][1000 genomes] |
rs1677736 | 0.83[EUR][1000 genomes] |
rs1677738 | 0.85[EUR][1000 genomes] |
rs1677739 | 0.84[EUR][1000 genomes] |
rs1748340 | 0.85[EUR][1000 genomes] |
rs1748341 | 0.85[EUR][1000 genomes] |
rs1748342 | 0.85[EUR][1000 genomes] |
rs1748343 | 0.85[EUR][1000 genomes] |
rs1748344 | 0.85[EUR][1000 genomes] |
rs1748345 | 0.85[EUR][1000 genomes] |
rs1748346 | 0.84[EUR][1000 genomes] |
rs1748347 | 0.86[EUR][1000 genomes] |
rs1748348 | 0.84[EUR][1000 genomes] |
rs1748349 | 0.83[EUR][1000 genomes] |
rs1748350 | 0.82[EUR][1000 genomes] |
rs1748351 | 0.82[EUR][1000 genomes] |
rs1780170 | 0.84[EUR][1000 genomes] |
rs1780171 | 0.84[EUR][1000 genomes] |
rs1780172 | 0.84[EUR][1000 genomes] |
rs1780173 | 0.84[EUR][1000 genomes] |
rs1780175 | 0.83[EUR][1000 genomes] |
rs1780178 | 0.86[EUR][1000 genomes] |
rs1780187 | 0.81[EUR][1000 genomes] |
rs1780188 | 0.82[EUR][1000 genomes] |
rs1809358 | 0.83[EUR][1000 genomes] |
rs1812155 | 0.83[EUR][1000 genomes] |
rs1871299 | 0.82[EUR][1000 genomes] |
rs1871300 | 0.84[EUR][1000 genomes] |
rs1947788 | 0.83[EUR][1000 genomes] |
rs2005118 | 0.93[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs2005119 | 0.93[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs2005253 | 0.84[EUR][1000 genomes] |
rs2011849 | 0.83[EUR][1000 genomes] |
rs2011860 | 0.83[EUR][1000 genomes] |
rs2224898 | 0.83[EUR][1000 genomes] |
rs2251814 | 0.90[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs2448109 | 0.93[AFR][1000 genomes];0.91[EUR][1000 genomes] |
rs2448110 | 0.93[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs2448112 | 0.82[EUR][1000 genomes] |
rs2448113 | 0.83[EUR][1000 genomes] |
rs2448114 | 0.83[EUR][1000 genomes] |
rs2448115 | 0.82[EUR][1000 genomes] |
rs2448116 | 0.83[EUR][1000 genomes] |
rs2448119 | 0.84[EUR][1000 genomes] |
rs2448120 | 0.83[EUR][1000 genomes] |
rs2448121 | 0.83[EUR][1000 genomes] |
rs2448122 | 0.85[EUR][1000 genomes] |
rs2448123 | 0.82[EUR][1000 genomes] |
rs2448124 | 0.81[EUR][1000 genomes] |
rs2448125 | 0.83[EUR][1000 genomes] |
rs2448128 | 0.84[EUR][1000 genomes] |
rs2448129 | 0.83[EUR][1000 genomes] |
rs2448131 | 0.84[EUR][1000 genomes] |
rs2477282 | 0.93[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs2477283 | 0.93[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs2477284 | 0.82[ASN][1000 genomes] |
rs2477286 | 0.84[EUR][1000 genomes] |
rs2477288 | 0.83[EUR][1000 genomes] |
rs2477289 | 0.84[EUR][1000 genomes] |
rs2477290 | 0.84[EUR][1000 genomes] |
rs2477291 | 0.83[EUR][1000 genomes] |
rs2477293 | 0.83[EUR][1000 genomes] |
rs2489558 | 0.86[EUR][1000 genomes] |
rs2489584 | 0.83[EUR][1000 genomes] |
rs2489585 | 0.82[EUR][1000 genomes] |
rs2489586 | 0.84[EUR][1000 genomes] |
rs2489587 | 0.84[EUR][1000 genomes] |
rs2489588 | 0.84[EUR][1000 genomes] |
rs2489590 | 0.84[EUR][1000 genomes] |
rs2489591 | 0.83[EUR][1000 genomes] |
rs2489592 | 0.83[EUR][1000 genomes] |
rs2489593 | 0.83[EUR][1000 genomes] |
rs2489594 | 0.82[EUR][1000 genomes] |
rs2489595 | 0.81[EUR][1000 genomes] |
rs2489596 | 0.85[EUR][1000 genomes] |
rs2489597 | 0.83[EUR][1000 genomes] |
rs2489600 | 0.84[EUR][1000 genomes] |
rs2489601 | 0.84[EUR][1000 genomes] |
rs2489602 | 0.92[AFR][1000 genomes];0.92[EUR][1000 genomes] |
rs2489603 | 0.92[EUR][1000 genomes] |
rs2860415 | 0.91[EUR][1000 genomes] |
rs3101794 | 0.83[EUR][1000 genomes] |
rs3118159 | 0.85[EUR][1000 genomes] |
rs3118160 | 0.84[EUR][1000 genomes] |
rs3121616 | 0.85[EUR][1000 genomes] |
rs3121618 | 0.83[EUR][1000 genomes] |
rs4749176 | 0.83[EUR][1000 genomes] |
rs7905832 | 0.90[EUR][1000 genomes] |
rs7910625 | 0.83[EUR][1000 genomes] |
rs7914153 | 0.84[EUR][1000 genomes] |
rs899374 | 0.84[EUR][1000 genomes] |
rs9417486 | 0.80[EUR][1000 genomes] |
rs9418574 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv894975 | chr10:26343356-27014467 | Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
2 | esv3436664 | chr10:26860755-26969397 | Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv1041766 | chr10:26890945-26969381 | Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv1046911 | chr10:26894348-26969381 | Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
5 | nsv1044057 | chr10:26894348-26971879 | Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
6 | nsv516275 | chr10:26896432-26968171 | Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
7 | esv3333006 | chr10:26908323-26985227 | Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | esv3353004 | chr10:26912762-26966282 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
9 | esv3415799 | chr10:26929831-27233591 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:26963200-26965200 | Active TSS | K562 | blood |
2 | chr10:26963400-26969400 | Weak transcription | Thymus | Thymus |