Variant report
Variant | rs2733284 |
---|---|
Chromosome Location | chr12:41936038-41936039 |
allele | A/C |
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] |
---|---|
rs1026464 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs10785265 | 0.80[EUR][1000 genomes] |
rs10880075 | 0.82[EUR][1000 genomes] |
rs10880076 | 0.83[EUR][1000 genomes] |
rs11180999 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11181001 | 0.81[CHB][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1155220 | 0.82[EUR][1000 genomes] |
rs1160183 | 0.81[EUR][1000 genomes] |
rs1160184 | 0.82[EUR][1000 genomes] |
rs1160748 | 0.82[EUR][1000 genomes] |
rs1160749 | 0.82[EUR][1000 genomes] |
rs1350429 | 0.82[EUR][1000 genomes] |
rs1379758 | 0.86[EUR][1000 genomes] |
rs1379759 | 0.86[EUR][1000 genomes] |
rs1379760 | 0.86[EUR][1000 genomes] |
rs1379761 | 0.84[EUR][1000 genomes] |
rs1379763 | 0.85[EUR][1000 genomes] |
rs1379764 | 0.84[EUR][1000 genomes] |
rs1379768 | 0.80[EUR][1000 genomes] |
rs1379769 | 0.85[EUR][1000 genomes] |
rs1379770 | 0.84[EUR][1000 genomes] |
rs1379771 | 0.85[EUR][1000 genomes] |
rs1379772 | 0.85[EUR][1000 genomes] |
rs1379773 | 0.83[EUR][1000 genomes] |
rs1379774 | 0.86[EUR][1000 genomes] |
rs1379776 | 0.82[EUR][1000 genomes] |
rs1458156 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1458157 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1458158 | 0.91[EUR][1000 genomes] |
rs1458159 | 0.84[EUR][1000 genomes] |
rs1458160 | 0.88[EUR][1000 genomes] |
rs1458166 | 0.82[EUR][1000 genomes] |
rs1458167 | 0.82[EUR][1000 genomes] |
rs1458168 | 0.82[EUR][1000 genomes] |
rs1471161 | 0.83[EUR][1000 genomes] |
rs1471162 | 0.82[EUR][1000 genomes] |
rs1471163 | 0.82[EUR][1000 genomes] |
rs1551593 | 0.83[EUR][1000 genomes] |
rs1551595 | 0.82[EUR][1000 genomes] |
rs1551596 | 0.82[EUR][1000 genomes] |
rs1598894 | 0.82[EUR][1000 genomes] |
rs1841025 | 0.82[EUR][1000 genomes] |
rs1870285 | 0.85[EUR][1000 genomes] |
rs1870286 | 0.85[EUR][1000 genomes] |
rs1902906 | 0.86[EUR][1000 genomes] |
rs2034923 | 0.91[EUR][1000 genomes] |
rs2125286 | 0.86[EUR][1000 genomes] |
rs2125287 | 0.86[EUR][1000 genomes] |
rs2199028 | 0.89[EUR][1000 genomes] |
rs2250003 | 0.86[EUR][1000 genomes] |
rs2250009 | 0.86[EUR][1000 genomes] |
rs2250908 | 0.82[EUR][1000 genomes] |
rs2251259 | 0.82[EUR][1000 genomes] |
rs2251349 | 0.82[EUR][1000 genomes] |
rs2251672 | 0.80[EUR][1000 genomes] |
rs2251683 | 0.82[EUR][1000 genomes] |
rs2251684 | 0.81[EUR][1000 genomes] |
rs2253528 | 0.88[EUR][1000 genomes] |
rs2253633 | 0.86[EUR][1000 genomes] |
rs2253634 | 0.88[EUR][1000 genomes] |
rs2255035 | 0.85[EUR][1000 genomes] |
rs2255145 | 0.85[EUR][1000 genomes] |
rs2255152 | 0.84[EUR][1000 genomes] |
rs2255404 | 0.86[EUR][1000 genomes] |
rs2256412 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2264905 | 0.82[EUR][1000 genomes] |
rs2405920 | 0.86[EUR][1000 genomes] |
rs2405921 | 0.86[EUR][1000 genomes] |
rs2446143 | 0.82[EUR][1000 genomes] |
rs2446144 | 0.82[EUR][1000 genomes] |
rs2468310 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2468314 | 0.88[EUR][1000 genomes] |
rs2468315 | 0.86[EUR][1000 genomes] |
rs2468316 | 0.86[EUR][1000 genomes] |
rs2468317 | 0.86[EUR][1000 genomes] |
rs2608689 | 0.86[EUR][1000 genomes] |
rs2608690 | 0.86[EUR][1000 genomes] |
rs2608691 | 0.85[EUR][1000 genomes] |
rs2608692 | 0.85[EUR][1000 genomes] |
rs2608696 | 0.85[EUR][1000 genomes] |
rs2608697 | 0.85[EUR][1000 genomes] |
rs2608701 | 0.82[EUR][1000 genomes] |
rs2608702 | 0.84[EUR][1000 genomes] |
rs2608704 | 0.85[EUR][1000 genomes] |
rs2608705 | 0.85[EUR][1000 genomes] |
rs2608706 | 0.85[EUR][1000 genomes] |
rs2608707 | 0.82[EUR][1000 genomes] |
rs2608708 | 0.84[EUR][1000 genomes] |
rs2608710 | 0.82[EUR][1000 genomes] |
rs2608711 | 0.86[EUR][1000 genomes] |
rs2608714 | 0.86[EUR][1000 genomes] |
rs2608715 | 0.88[EUR][1000 genomes] |
rs2608716 | 0.87[EUR][1000 genomes] |
rs2608717 | 0.86[JPT][hapmap] |
rs2608718 | 0.86[EUR][1000 genomes] |
rs2710264 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2710265 | 0.87[ASN][1000 genomes] |
rs2730802 | 0.85[EUR][1000 genomes] |
rs2730803 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2730805 | 0.84[EUR][1000 genomes] |
rs2730807 | 0.87[EUR][1000 genomes] |
rs2730809 | 0.82[EUR][1000 genomes] |
rs2730810 | 0.83[EUR][1000 genomes] |
rs2730811 | 0.82[EUR][1000 genomes] |
rs2730814 | 0.89[EUR][1000 genomes] |
rs2730817 | 0.82[EUR][1000 genomes] |
rs2730818 | 0.81[EUR][1000 genomes] |
rs2730819 | 0.82[EUR][1000 genomes] |
rs2730820 | 0.82[EUR][1000 genomes] |
rs2730821 | 0.82[EUR][1000 genomes] |
rs2730822 | 0.82[EUR][1000 genomes] |
rs2730824 | 0.86[EUR][1000 genomes] |
rs2730827 | 0.88[EUR][1000 genomes] |
rs2730828 | 0.83[EUR][1000 genomes] |
rs2730829 | 0.82[EUR][1000 genomes] |
rs2730830 | 0.83[EUR][1000 genomes] |
rs2733274 | 0.82[EUR][1000 genomes] |
rs2733275 | 0.88[EUR][1000 genomes] |
rs2733276 | 0.86[EUR][1000 genomes] |
rs2733278 | 0.88[EUR][1000 genomes] |
rs2733280 | 0.88[EUR][1000 genomes] |
rs2733282 | 0.81[EUR][1000 genomes] |
rs2733285 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2733287 | 0.91[EUR][1000 genomes] |
rs2733289 | 0.81[EUR][1000 genomes] |
rs2733290 | 0.83[EUR][1000 genomes] |
rs2733291 | 0.80[EUR][1000 genomes] |
rs2733292 | 0.81[EUR][1000 genomes] |
rs2733293 | 0.81[EUR][1000 genomes] |
rs2733297 | 0.82[EUR][1000 genomes] |
rs2733298 | 0.85[EUR][1000 genomes] |
rs2733299 | 0.85[EUR][1000 genomes] |
rs285553 | 0.82[JPT][hapmap] |
rs285556 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs285557 | 0.90[ASN][1000 genomes] |
rs285558 | 0.83[JPT][hapmap] |
rs285560 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs285574 | 0.81[CHB][hapmap];0.86[JPT][hapmap] |
rs285575 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs285590 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs285592 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs285593 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs285595 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2957590 | 0.82[EUR][1000 genomes] |
rs389166 | 0.81[CHB][hapmap] |
rs437178 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4584644 | 0.80[EUR][1000 genomes] |
rs4768354 | 0.83[EUR][1000 genomes] |
rs7298808 | 0.81[EUR][1000 genomes] |
rs7954518 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs897973 | 0.82[EUR][1000 genomes] |
rs981012 | 0.82[EUR][1000 genomes] |
rs981014 | 0.83[EUR][1000 genomes] |
rs989904 | 0.80[EUR][1000 genomes] |
rs996356 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832384 | chr12:41772648-41971430 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv3337301 | chr12:41851654-42093677 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv899040 | chr12:41905897-42181706 | Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:41925600-41949800 | Weak transcription | Stomach Smooth Muscle | stomach |
2 | chr12:41925800-41944800 | Weak transcription | Brain Germinal Matrix | brain |