Variant report
Variant | rs17442735 |
---|---|
Chromosome Location | chr12:40536470-40536471 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-SLC2A13-1 | chr12:40534728-40536678 | ENSG00000260943.1 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10747955 | 1.00[ASN][1000 genomes] |
rs10747959 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10784283 | 1.00[ASN][1000 genomes] |
rs10878226 | 0.85[YRI][hapmap] |
rs10878244 | 0.82[YRI][hapmap] |
rs10878246 | 1.00[YRI][hapmap] |
rs11175620 | 0.85[YRI][hapmap] |
rs11175645 | 0.85[YRI][hapmap] |
rs11175655 | 1.00[YRI][hapmap] |
rs11175658 | 0.85[YRI][hapmap] |
rs11175666 | 0.85[YRI][hapmap] |
rs11564118 | 0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11564120 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11564122 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11564128 | 1.00[JPT][hapmap] |
rs11564132 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11564204 | 1.00[JPT][hapmap] |
rs11564226 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11564274 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11564275 | 0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12099949 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12368785 | 1.00[JPT][hapmap] |
rs12368891 | 1.00[JPT][hapmap] |
rs1497046 | 1.00[ASN][1000 genomes] |
rs1497048 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1566127 | 1.00[ASN][1000 genomes] |
rs17442206 | 1.00[JPT][hapmap] |
rs17442297 | 1.00[JPT][hapmap] |
rs17442665 | 0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17442742 | 1.00[JPT][hapmap] |
rs17442812 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17442853 | 1.00[YRI][hapmap] |
rs17442980 | 1.00[JPT][hapmap] |
rs17443178 | 1.00[JPT][hapmap] |
rs17443185 | 1.00[JPT][hapmap] |
rs17443206 | 1.00[JPT][hapmap] |
rs17443366 | 1.00[JPT][hapmap] |
rs17443380 | 1.00[JPT][hapmap] |
rs17443387 | 1.00[JPT][hapmap] |
rs17443504 | 1.00[JPT][hapmap] |
rs17443882 | 1.00[JPT][hapmap] |
rs17443916 | 1.00[JPT][hapmap] |
rs17443951 | 1.00[JPT][hapmap] |
rs17444021 | 1.00[JPT][hapmap] |
rs17444033 | 1.00[JPT][hapmap] |
rs17458093 | 1.00[JPT][hapmap] |
rs17458121 | 1.00[JPT][hapmap] |
rs17458202 | 1.00[JPT][hapmap] |
rs17458341 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17458396 | 1.00[JPT][hapmap] |
rs17458417 | 1.00[JPT][hapmap] |
rs17458487 | 1.00[JPT][hapmap] |
rs17458528 | 1.00[JPT][hapmap] |
rs17458780 | 0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17458836 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17458974 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17461337 | 1.00[JPT][hapmap] |
rs17465428 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17465737 | 1.00[JPT][hapmap] |
rs17465751 | 1.00[JPT][hapmap] |
rs17465807 | 1.00[JPT][hapmap] |
rs17465877 | 1.00[JPT][hapmap] |
rs17466002 | 1.00[JPT][hapmap] |
rs17466143 | 1.00[JPT][hapmap] |
rs17466206 | 1.00[JPT][hapmap] |
rs17466213 | 1.00[JPT][hapmap] |
rs17466241 | 1.00[JPT][hapmap] |
rs17466458 | 1.00[JPT][hapmap] |
rs17466514 | 1.00[JPT][hapmap] |
rs17466535 | 1.00[JPT][hapmap] |
rs17483857 | 1.00[JPT][hapmap] |
rs17483996 | 1.00[JPT][hapmap] |
rs17484176 | 1.00[JPT][hapmap] |
rs17489170 | 1.00[JPT][hapmap] |
rs17489218 | 1.00[JPT][hapmap] |
rs17489225 | 1.00[JPT][hapmap] |
rs17489246 | 1.00[JPT][hapmap] |
rs17489253 | 1.00[JPT][hapmap] |
rs17489267 | 1.00[JPT][hapmap] |
rs17489365 | 1.00[JPT][hapmap] |
rs17489410 | 1.00[JPT][hapmap] |
rs17489417 | 1.00[JPT][hapmap] |
rs17489466 | 1.00[JPT][hapmap] |
rs17489501 | 1.00[JPT][hapmap] |
rs17489583 | 1.00[JPT][hapmap] |
rs17489590 | 1.00[JPT][hapmap] |
rs17489597 | 1.00[JPT][hapmap] |
rs17489638 | 1.00[JPT][hapmap] |
rs17489869 | 1.00[JPT][hapmap] |
rs17489985 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17490006 | 1.00[JPT][hapmap] |
rs17490334 | 1.00[JPT][hapmap] |
rs17490341 | 1.00[JPT][hapmap] |
rs17490599 | 1.00[JPT][hapmap] |
rs17490769 | 1.00[JPT][hapmap] |
rs17490796 | 1.00[JPT][hapmap] |
rs17490810 | 1.00[JPT][hapmap] |
rs17491047 | 1.00[JPT][hapmap] |
rs17491061 | 1.00[JPT][hapmap] |
rs17491068 | 1.00[JPT][hapmap] |
rs17491180 | 1.00[JPT][hapmap] |
rs17491340 | 1.00[JPT][hapmap] |
rs17491445 | 1.00[JPT][hapmap] |
rs17491515 | 1.00[JPT][hapmap] |
rs17491529 | 1.00[JPT][hapmap] |
rs17518057 | 1.00[JPT][hapmap] |
rs17518071 | 1.00[JPT][hapmap] |
rs17518141 | 1.00[JPT][hapmap] |
rs17518148 | 1.00[JPT][hapmap] |
rs17518155 | 1.00[JPT][hapmap] |
rs17518204 | 1.00[JPT][hapmap] |
rs17518232 | 1.00[JPT][hapmap] |
rs17518343 | 1.00[JPT][hapmap] |
rs17518413 | 1.00[JPT][hapmap] |
rs17518420 | 1.00[JPT][hapmap] |
rs17518532 | 1.00[JPT][hapmap] |
rs17518910 | 1.00[JPT][hapmap] |
rs17519531 | 1.00[JPT][hapmap] |
rs17519566 | 1.00[JPT][hapmap] |
rs17519573 | 0.85[YRI][hapmap] |
rs17519580 | 1.00[JPT][hapmap] |
rs17519615 | 1.00[JPT][hapmap] |
rs17519671 | 1.00[JPT][hapmap] |
rs17519811 | 1.00[JPT][hapmap] |
rs17519825 | 1.00[JPT][hapmap] |
rs17519832 | 1.00[JPT][hapmap] |
rs17519985 | 1.00[JPT][hapmap] |
rs17520020 | 1.00[JPT][hapmap] |
rs17520278 | 1.00[JPT][hapmap] |
rs17520292 | 1.00[JPT][hapmap] |
rs2132745 | 1.00[ASN][1000 genomes] |
rs2132746 | 1.00[ASN][1000 genomes] |
rs2404351 | 1.00[ASN][1000 genomes] |
rs28365178 | 1.00[JPT][hapmap] |
rs28365191 | 1.00[JPT][hapmap] |
rs28365203 | 1.00[JPT][hapmap] |
rs28365211 | 1.00[JPT][hapmap] |
rs28365221 | 1.00[JPT][hapmap] |
rs28365226 | 1.00[JPT][hapmap] |
rs28365682 | 1.00[JPT][hapmap] |
rs28365690 | 1.00[JPT][hapmap] |
rs28370599 | 1.00[ASN][1000 genomes] |
rs28370601 | 1.00[JPT][hapmap] |
rs28370605 | 1.00[JPT][hapmap] |
rs28370608 | 1.00[JPT][hapmap] |
rs28370616 | 1.00[JPT][hapmap] |
rs28370643 | 1.00[JPT][hapmap] |
rs28370649 | 1.00[JPT][hapmap] |
rs28370652 | 1.00[JPT][hapmap] |
rs28370655 | 1.00[JPT][hapmap] |
rs28370658 | 1.00[JPT][hapmap] |
rs28370665 | 1.00[JPT][hapmap] |
rs28370670 | 1.00[JPT][hapmap] |
rs28370672 | 1.00[JPT][hapmap] |
rs28370673 | 1.00[JPT][hapmap] |
rs28370682 | 1.00[JPT][hapmap] |
rs28370686 | 1.00[JPT][hapmap] |
rs28370690 | 1.00[JPT][hapmap] |
rs28370692 | 1.00[JPT][hapmap] |
rs28370696 | 1.00[JPT][hapmap] |
rs28370700 | 1.00[JPT][hapmap] |
rs28370707 | 1.00[JPT][hapmap] |
rs28370718 | 1.00[JPT][hapmap] |
rs28370731 | 1.00[JPT][hapmap] |
rs28370737 | 1.00[JPT][hapmap] |
rs28370744 | 1.00[JPT][hapmap] |
rs28370750 | 1.00[JPT][hapmap] |
rs28370751 | 1.00[JPT][hapmap] |
rs28370755 | 1.00[JPT][hapmap] |
rs28370764 | 1.00[JPT][hapmap] |
rs28370765 | 1.00[JPT][hapmap] |
rs28370767 | 1.00[JPT][hapmap] |
rs28370768 | 1.00[JPT][hapmap] |
rs28370771 | 1.00[JPT][hapmap] |
rs28370772 | 1.00[JPT][hapmap] |
rs28370776 | 1.00[JPT][hapmap] |
rs28370779 | 1.00[JPT][hapmap] |
rs28370787 | 1.00[JPT][hapmap] |
rs28370793 | 1.00[JPT][hapmap] |
rs28370796 | 1.00[JPT][hapmap] |
rs28370800 | 1.00[JPT][hapmap] |
rs28370806 | 1.00[JPT][hapmap] |
rs28370808 | 1.00[JPT][hapmap] |
rs28370813 | 1.00[JPT][hapmap] |
rs28370818 | 1.00[JPT][hapmap] |
rs28370823 | 1.00[JPT][hapmap] |
rs28370826 | 1.00[JPT][hapmap] |
rs2952711 | 0.83[EUR][1000 genomes] |
rs34714539 | 1.00[ASN][1000 genomes] |
rs35985096 | 1.00[ASN][1000 genomes] |
rs4768196 | 1.00[ASN][1000 genomes] |
rs4768202 | 1.00[ASN][1000 genomes] |
rs6581438 | 1.00[ASN][1000 genomes] |
rs6581439 | 1.00[ASN][1000 genomes] |
rs7135678 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[YRI][hapmap];0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7138075 | 1.00[ASN][1000 genomes] |
rs7138078 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs71449744 | 1.00[ASN][1000 genomes] |
rs7294619 | 0.85[YRI][hapmap] |
rs7300161 | 0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7305155 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7305994 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs74088117 | 1.00[ASN][1000 genomes] |
rs7959787 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs937385 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv558596 | chr12:40413698-40591117 | Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | esv1836585 | chr12:40492814-40540939 | Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | esv1839483 | chr12:40492814-40540939 | Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | nsv899030 | chr12:40509341-40580440 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
5 | nsv899031 | chr12:40520684-40580440 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
6 | nsv519063 | chr12:40536061-40538858 | Enhancers Weak transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:40532800-40543800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr12:40535000-40537200 | Enhancers | Hela-S3 | cervix |
3 | chr12:40535600-40536600 | Enhancers | HMEC | breast |
4 | chr12:40535600-40536600 | Enhancers | NHEK | skin |
5 | chr12:40536000-40536600 | Enhancers | Placenta Amnion | Placenta Amnion |