Variant report
Variant | rs10141692 |
---|---|
Chromosome Location | chr14:67695017-67695018 |
allele | A/G |
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:
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Variant related genes | Relation type |
---|---|
ENSG00000072415 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10129779 | 0.83[ASN][1000 genomes] |
rs10130796 | 0.85[ASN][1000 genomes] |
rs10131212 | 0.80[ASN][1000 genomes] |
rs10135883 | 0.88[ASN][1000 genomes] |
rs10135903 | 0.81[ASN][1000 genomes] |
rs10138319 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10138824 | 0.80[ASN][1000 genomes] |
rs10138932 | 0.80[ASN][1000 genomes] |
rs10140817 | 0.83[ASN][1000 genomes] |
rs10141879 | 0.93[ASN][1000 genomes] |
rs10143916 | 0.83[ASN][1000 genomes] |
rs10144090 | 0.89[ASN][1000 genomes] |
rs10144218 | 0.90[ASN][1000 genomes] |
rs10144401 | 0.81[ASN][1000 genomes] |
rs10145586 | 0.90[ASN][1000 genomes] |
rs10145744 | 0.91[ASN][1000 genomes] |
rs10146663 | 0.81[ASN][1000 genomes] |
rs10146722 | 0.80[ASN][1000 genomes] |
rs10147852 | 0.91[ASN][1000 genomes] |
rs10150082 | 0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs10150902 | 0.81[ASN][1000 genomes] |
rs10151464 | 0.83[ASN][1000 genomes] |
rs10152002 | 0.91[ASN][1000 genomes] |
rs1044750 | 0.81[ASN][1000 genomes] |
rs10459453 | 0.90[ASN][1000 genomes] |
rs10459529 | 0.90[ASN][1000 genomes] |
rs10459530 | 0.89[ASN][1000 genomes] |
rs10459531 | 0.90[ASN][1000 genomes] |
rs1073604 | 0.92[ASN][1000 genomes] |
rs1073605 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1073606 | 0.90[ASN][1000 genomes] |
rs1073607 | 0.90[ASN][1000 genomes] |
rs1078194 | 0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10873200 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs1113973 | 0.90[ASN][1000 genomes] |
rs11158655 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs11158656 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11158658 | 0.89[ASN][1000 genomes] |
rs12323494 | 0.89[ASN][1000 genomes] |
rs12323793 | 0.84[ASN][1000 genomes] |
rs12323911 | 0.90[ASN][1000 genomes] |
rs12586402 | 0.85[ASN][1000 genomes] |
rs12586552 | 0.81[ASN][1000 genomes] |
rs12586609 | 0.80[ASN][1000 genomes] |
rs12588355 | 0.80[ASN][1000 genomes] |
rs12588388 | 0.80[ASN][1000 genomes] |
rs12589218 | 0.90[ASN][1000 genomes] |
rs12589325 | 0.88[ASN][1000 genomes] |
rs12589606 | 0.80[ASN][1000 genomes] |
rs12590956 | 0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes] |
rs1318914 | 0.89[ASN][1000 genomes] |
rs1473733 | 0.81[ASN][1000 genomes] |
rs1475127 | 0.91[ASN][1000 genomes] |
rs1475128 | 0.80[ASN][1000 genomes] |
rs1475129 | 0.80[ASN][1000 genomes] |
rs1535489 | 0.83[ASN][1000 genomes] |
rs1535490 | 0.83[ASN][1000 genomes] |
rs1535491 | 0.83[ASN][1000 genomes] |
rs17093616 | 0.81[ASN][1000 genomes] |
rs17104103 | 0.82[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs17104106 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs17104109 | 0.85[ASN][1000 genomes] |
rs17104114 | 0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs17104188 | 0.90[ASN][1000 genomes] |
rs17104223 | 0.81[ASN][1000 genomes] |
rs17104224 | 0.81[ASN][1000 genomes] |
rs17248456 | 0.95[ASN][1000 genomes] |
rs17248526 | 0.90[ASN][1000 genomes] |
rs17248567 | 0.83[ASN][1000 genomes] |
rs17836683 | 0.89[ASN][1000 genomes] |
rs17836702 | 0.80[ASN][1000 genomes] |
rs1881035 | 0.91[ASN][1000 genomes] |
rs1885589 | 0.80[ASN][1000 genomes] |
rs1918484 | 0.85[ASN][1000 genomes] |
rs2025208 | 0.90[ASN][1000 genomes] |
rs2025209 | 0.88[ASN][1000 genomes] |
rs2057396 | 0.80[ASN][1000 genomes] |
rs2146229 | 0.83[ASN][1000 genomes] |
rs2146230 | 0.90[ASN][1000 genomes] |
rs28370351 | 0.91[ASN][1000 genomes] |
rs28401319 | 0.90[ASN][1000 genomes] |
rs28411190 | 0.91[ASN][1000 genomes] |
rs28424592 | 0.90[ASN][1000 genomes] |
rs28472807 | 0.81[ASN][1000 genomes] |
rs28521373 | 0.81[ASN][1000 genomes] |
rs28522593 | 0.91[ASN][1000 genomes] |
rs28522922 | 0.87[ASN][1000 genomes] |
rs28562402 | 0.91[ASN][1000 genomes] |
rs28584286 | 0.81[ASN][1000 genomes] |
rs28607485 | 0.83[ASN][1000 genomes] |
rs28617290 | 0.81[ASN][1000 genomes] |
rs28696352 | 0.89[ASN][1000 genomes] |
rs28706091 | 0.80[ASN][1000 genomes] |
rs3784081 | 0.83[ASN][1000 genomes] |
rs3809387 | 0.80[ASN][1000 genomes] |
rs3844530 | 0.81[ASN][1000 genomes] |
rs4058254 | 0.81[ASN][1000 genomes] |
rs45612334 | 0.91[ASN][1000 genomes] |
rs4636843 | 0.81[ASN][1000 genomes] |
rs57025434 | 0.83[ASN][1000 genomes] |
rs57266997 | 0.90[ASN][1000 genomes] |
rs57782535 | 0.90[ASN][1000 genomes] |
rs58809332 | 0.90[ASN][1000 genomes] |
rs58954149 | 0.90[ASN][1000 genomes] |
rs59472119 | 0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs59861720 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs60953279 | 0.90[ASN][1000 genomes] |
rs61024303 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs61281789 | 0.89[ASN][1000 genomes] |
rs61510566 | 0.90[ASN][1000 genomes] |
rs61612119 | 0.86[ASN][1000 genomes] |
rs61749574 | 0.89[ASN][1000 genomes] |
rs6573758 | 0.87[ASN][1000 genomes] |
rs6573760 | 0.88[ASN][1000 genomes] |
rs6573763 | 0.92[ASN][1000 genomes] |
rs6573764 | 0.90[ASN][1000 genomes] |
rs67470433 | 0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7140287 | 0.90[ASN][1000 genomes] |
rs7144928 | 0.81[ASN][1000 genomes] |
rs7149535 | 0.90[ASN][1000 genomes] |
rs7151684 | 0.89[ASN][1000 genomes] |
rs7152903 | 0.90[ASN][1000 genomes] |
rs7153965 | 0.80[ASN][1000 genomes] |
rs7158743 | 0.81[ASN][1000 genomes] |
rs7158751 | 0.80[ASN][1000 genomes] |
rs7160238 | 0.80[ASN][1000 genomes] |
rs73276994 | 0.82[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs73279028 | 0.91[ASN][1000 genomes] |
rs73279056 | 0.94[ASN][1000 genomes] |
rs73280932 | 0.92[ASN][1000 genomes] |
rs73280967 | 0.90[ASN][1000 genomes] |
rs73282706 | 0.82[ASN][1000 genomes] |
rs73282711 | 0.83[ASN][1000 genomes] |
rs73282717 | 0.81[ASN][1000 genomes] |
rs73282746 | 0.81[ASN][1000 genomes] |
rs73282772 | 0.80[ASN][1000 genomes] |
rs73282775 | 0.80[ASN][1000 genomes] |
rs73282776 | 0.80[ASN][1000 genomes] |
rs73282798 | 0.80[ASN][1000 genomes] |
rs8003669 | 0.94[ASN][1000 genomes] |
rs8004148 | 0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs8004488 | 0.87[ASN][1000 genomes] |
rs8008155 | 0.89[ASN][1000 genomes] |
rs8008236 | 0.90[ASN][1000 genomes] |
rs8008443 | 0.84[ASN][1000 genomes] |
rs8009318 | 0.91[ASN][1000 genomes] |
rs8014104 | 0.83[ASN][1000 genomes] |
rs8014259 | 0.83[ASN][1000 genomes] |
rs8014966 | 0.80[ASN][1000 genomes] |
rs8016037 | 0.90[ASN][1000 genomes] |
rs8017301 | 0.90[ASN][1000 genomes] |
rs8018738 | 0.91[ASN][1000 genomes] |
rs8021896 | 0.83[ASN][1000 genomes] |
rs8021992 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9323496 | 0.91[ASN][1000 genomes] |
rs9743911 | 0.90[ASN][1000 genomes] |
rs9743912 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv902058 | chr14:67310195-67760538 | Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv902059 | chr14:67352226-67760538 | ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
3 | esv2751285 | chr14:67364747-67886781 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
4 | nsv902060 | chr14:67417083-67760538 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
5 | nsv1045518 | chr14:67529049-67959582 | Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
6 | nsv832821 | chr14:67590418-67828169 | Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
7 | nsv1040257 | chr14:67634585-67762806 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:67687000-67697000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr14:67689400-67695200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr14:67689400-67695200 | Weak transcription | NH-A | brain |
4 | chr14:67689400-67695400 | Weak transcription | HSMM | muscle |
5 | chr14:67692800-67695200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
6 | chr14:67692800-67698400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
7 | chr14:67694200-67698800 | Weak transcription | NHEK | skin |
8 | chr14:67695000-67695200 | Enhancers | Muscle Satellite Cultured Cells | -- |
9 | chr14:67695000-67695200 | Active TSS | A549 | lung |
10 | chr14:67695000-67695400 | Active TSS | Stomach Smooth Muscle | stomach |
11 | chr14:67695000-67695800 | Active TSS | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |