Variant report
Variant | rs28504496 |
---|---|
Chromosome Location | chr15:44016883-44016884 |
allele | C/T |
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 |
---|---|
ENSG00000166762 | Chromatin interaction |
ENSG00000206991 | Chromatin interaction |
ENSG00000067369 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10163054 | 0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10438303 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11070407 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11070408 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11070410 | 0.85[ASN][1000 genomes] |
rs11852840 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11856184 | 0.80[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs11857661 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12101756 | 0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12437808 | 0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12440573 | 0.83[AMR][1000 genomes] |
rs12441127 | 0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12441861 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12442129 | 0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12443102 | 0.87[EUR][1000 genomes] |
rs12702 | 0.86[AMR][1000 genomes] |
rs13380397 | 0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs16950562 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs16963953 | 0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs2228368 | 0.86[AMR][1000 genomes] |
rs2277531 | 0.83[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs2412810 | 0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2447193 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2447208 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2447211 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2447212 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2467402 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2467426 | 0.88[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2470121 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2788 | 0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28433760 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs28502289 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs28542007 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs28546844 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs28578041 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28578398 | 0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28583806 | 0.86[AMR][1000 genomes] |
rs28595038 | 0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs28606452 | 0.87[EUR][1000 genomes] |
rs28674750 | 0.86[AMR][1000 genomes] |
rs28678901 | 0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs28684672 | 0.83[AMR][1000 genomes] |
rs28718261 | 0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs28891769 | 0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2915776 | 0.84[EUR][1000 genomes] |
rs2915779 | 0.84[EUR][1000 genomes] |
rs2915792 | 0.81[EUR][1000 genomes] |
rs2920781 | 0.84[EUR][1000 genomes] |
rs2927072 | 0.80[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs2927075 | 0.86[EUR][1000 genomes] |
rs2957637 | 0.80[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs35457073 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3736180 | 0.85[AMR][1000 genomes] |
rs3759791 | 0.86[AMR][1000 genomes] |
rs3825783 | 0.85[AMR][1000 genomes] |
rs4332723 | 0.99[ASN][1000 genomes] |
rs4997480 | 0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs56008017 | 0.81[AMR][1000 genomes] |
rs57865312 | 0.87[EUR][1000 genomes] |
rs60883262 | 0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs62018952 | 0.84[ASN][1000 genomes] |
rs7167976 | 0.89[AFR][1000 genomes] |
rs7168158 | 0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7169988 | 0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7170167 | 0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7171750 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7174208 | 0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7174732 | 0.93[ASN][1000 genomes] |
rs7175032 | 0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7175129 | 0.99[ASN][1000 genomes] |
rs7180818 | 0.83[ASN][1000 genomes] |
rs72714307 | 0.84[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs8023696 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs8029210 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs8030169 | 0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs8033846 | 0.90[ASN][1000 genomes] |
rs8033995 | 0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs8042868 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1846172 | chr15:43632138-44116986 | Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 101 gene(s) | inside rSNPs | diseases |
2 | esv1846701 | chr15:43759774-44116986 | Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 90 gene(s) | inside rSNPs | diseases |
3 | esv2758379 | chr15:43823158-44148641 | Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 84 gene(s) | inside rSNPs | diseases |
4 | esv2760028 | chr15:43823158-44148641 | Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 84 gene(s) | inside rSNPs | diseases |
5 | nsv427960 | chr15:43823158-44148641 | Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 84 gene(s) | inside rSNPs | diseases |
6 | esv2757598 | chr15:43831923-44058634 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
7 | nsv904150 | chr15:43836478-44040965 | Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
8 | esv2760393 | chr15:43845422-44024490 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
9 | nsv904157 | chr15:43852043-44019592 | Bivalent Enhancer Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
10 | nsv904158 | chr15:43852043-44053617 | Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
11 | nsv904163 | chr15:43873489-44023963 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
12 | nsv1037786 | chr15:43888926-44318587 | Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 90 gene(s) | inside rSNPs | diseases |
13 | nsv542370 | chr15:43888926-44318587 | Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 90 gene(s) | inside rSNPs | diseases |
14 | nsv1038991 | chr15:43914737-44024490 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
15 | nsv1047213 | chr15:43929339-44024490 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 18 gene(s) | inside rSNPs | diseases |
16 | nsv431387 | chr15:43929378-44862930 | Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 158 gene(s) | inside rSNPs | diseases |
17 | nsv976928 | chr15:43948866-44040886 | Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
18 | nsv931051 | chr15:43988761-44833518 | Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 154 gene(s) | inside rSNPs | diseases |
19 | esv33661 | chr15:44016519-44064420 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs28504496 | ADAL | cis | Thyroid | GTEx |
rs28504496 | CATSPER2 | cis | Esophagus Mucosa | GTEx |
rs28504496 | ELL3 | Cis_1M | lymphoblastoid | RTeQTL |
rs28504496 | CATSPER2 | cis | lung | GTEx |
rs28504496 | ADAL | cis | lung | GTEx |
rs28504496 | CKMT1A | cis | Skin Sun Exposed Lower leg | GTEx |
rs28504496 | ADAL | cis | Artery Tibial | GTEx |
rs28504496 | CATSPER2 | cis | Whole Blood | GTEx |
rs28504496 | CKMT1A | cis | Esophagus Mucosa | GTEx |
rs28504496 | ADAL | cis | Esophagus Muscularis | GTEx |
rs28504496 | AC011330.5 | cis | Esophagus Mucosa | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:44013400-44037400 | Weak transcription | Fetal Intestine Small | intestine |