Variant report
Variant | rs72709307 |
---|---|
Chromosome Location | chr15:31906397-31906398 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11071196 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11071236 | 0.82[ASN][1000 genomes] |
rs11852462 | 0.85[ASN][1000 genomes] |
rs11856520 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12102147 | 0.80[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12898638 | 0.84[ASN][1000 genomes] |
rs12898981 | 0.83[ASN][1000 genomes] |
rs12899987 | 0.84[EUR][1000 genomes] |
rs12900146 | 0.82[ASN][1000 genomes] |
rs12900789 | 0.84[ASN][1000 genomes] |
rs12900803 | 0.84[ASN][1000 genomes] |
rs12901904 | 0.84[ASN][1000 genomes] |
rs12907373 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12907512 | 0.82[ASN][1000 genomes] |
rs12907720 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12909072 | 0.84[ASN][1000 genomes] |
rs12909183 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12909411 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12912683 | 0.81[EUR][1000 genomes] |
rs12913322 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12914358 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12914768 | 0.83[ASN][1000 genomes] |
rs13380159 | 0.83[ASN][1000 genomes] |
rs1459199 | 0.84[ASN][1000 genomes] |
rs1542453 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1813397 | 0.82[EUR][1000 genomes] |
rs2085667 | 0.84[ASN][1000 genomes] |
rs2100715 | 0.84[ASN][1000 genomes] |
rs2125624 | 0.84[ASN][1000 genomes] |
rs28525283 | 0.84[ASN][1000 genomes] |
rs2925 | 0.84[ASN][1000 genomes] |
rs34034041 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs34203834 | 0.84[ASN][1000 genomes] |
rs34268633 | 0.83[ASN][1000 genomes] |
rs34508606 | 0.81[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs34522308 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs34929828 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs34932530 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs35176167 | 0.84[EUR][1000 genomes] |
rs35257316 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs35353915 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs35474662 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs35546743 | 0.82[ASN][1000 genomes] |
rs4369619 | 0.84[ASN][1000 genomes] |
rs4584778 | 0.82[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs4591098 | 0.82[ASN][1000 genomes] |
rs4594225 | 0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4779543 | 0.84[ASN][1000 genomes] |
rs4779544 | 0.85[ASN][1000 genomes] |
rs4779894 | 0.82[EUR][1000 genomes] |
rs4779895 | 0.82[EUR][1000 genomes] |
rs4779899 | 0.82[ASN][1000 genomes] |
rs4779900 | 0.84[ASN][1000 genomes] |
rs4779901 | 0.84[ASN][1000 genomes] |
rs4779903 | 0.84[ASN][1000 genomes] |
rs4779905 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4779907 | 0.83[ASN][1000 genomes] |
rs4779909 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs57641116 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs58975032 | 0.84[EUR][1000 genomes] |
rs59059557 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs59597551 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs60011586 | 0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs60461663 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs67618202 | 0.83[ASN][1000 genomes] |
rs67932861 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs71401628 | 0.84[ASN][1000 genomes] |
rs71401629 | 0.84[ASN][1000 genomes] |
rs7162339 | 0.84[ASN][1000 genomes] |
rs7164729 | 0.80[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7165528 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7166285 | 0.82[ASN][1000 genomes] |
rs7167462 | 0.84[ASN][1000 genomes] |
rs7168828 | 0.82[ASN][1000 genomes] |
rs7169106 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7169637 | 0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7170060 | 0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7171081 | 0.84[ASN][1000 genomes] |
rs7171868 | 0.84[ASN][1000 genomes] |
rs7172593 | 0.86[ASN][1000 genomes] |
rs7176601 | 0.82[ASN][1000 genomes] |
rs7177069 | 0.80[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs7177083 | 0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7178026 | 0.83[ASN][1000 genomes] |
rs7183092 | 0.82[ASN][1000 genomes] |
rs7183472 | 0.83[ASN][1000 genomes] |
rs721548 | 0.82[EUR][1000 genomes] |
rs72726931 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7496104 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs8023393 | 0.83[ASN][1000 genomes] |
rs8023394 | 0.80[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs8023753 | 0.82[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs8024958 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs8025014 | 0.80[AMR][1000 genomes] |
rs8025024 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs8029308 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs8029454 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs8033168 | 0.81[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs8035863 | 0.82[ASN][1000 genomes] |
rs8036502 | 0.81[ASN][1000 genomes] |
rs8036561 | 0.82[ASN][1000 genomes] |
rs8040203 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs9302196 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs9672229 | 0.81[AMR][1000 genomes] |
rs9672933 | 0.81[AMR][1000 genomes] |
rs9744831 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs983242 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1054147 | chr15:31014507-31972706 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 87 gene(s) | inside rSNPs | diseases |
2 | nsv542306 | chr15:31014507-31972706 | Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 87 gene(s) | inside rSNPs | diseases |
3 | nsv1051589 | chr15:31728004-31972706 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv542320 | chr15:31728004-31972706 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv903845 | chr15:31751664-31939001 | Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | esv2422205 | chr15:31808878-32375021 | Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
7 | esv2422269 | chr15:31808878-32375021 | Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | esv2422351 | chr15:31808878-32375021 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
9 | esv2422455 | chr15:31808878-32375021 | Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
10 | nsv1045095 | chr15:31835044-32439113 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
11 | nsv903846 | chr15:31854847-32534037 | Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
12 | nsv469569 | chr15:31886000-31974400 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
13 | esv2751530 | chr15:31897012-32511555 | Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
14 | nsv976915 | chr15:31898697-31986377 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
15 | nsv1040340 | chr15:31900747-32439113 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:31902000-31908000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |