Variant report
Variant | rs4873407 |
---|---|
Chromosome Location | chr8:51044416-51044417 |
allele | G/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 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1000638 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1000639 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10096871 | 0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10098057 | 0.90[ASN][1000 genomes] |
rs10504094 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10504096 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10504098 | 0.91[ASN][1000 genomes] |
rs10957764 | 0.90[EUR][1000 genomes] |
rs10957802 | 0.94[EUR][1000 genomes] |
rs10957813 | 0.91[ASN][1000 genomes] |
rs10957814 | 0.91[ASN][1000 genomes] |
rs11775978 | 0.90[ASN][1000 genomes] |
rs11778998 | 0.88[ASN][1000 genomes] |
rs11780070 | 0.91[ASN][1000 genomes] |
rs11781981 | 0.93[ASN][1000 genomes] |
rs11786703 | 0.93[ASN][1000 genomes] |
rs11989367 | 0.81[ASN][1000 genomes] |
rs11991940 | 0.91[ASN][1000 genomes] |
rs12542067 | 0.83[ASN][1000 genomes] |
rs12545107 | 0.90[EUR][1000 genomes] |
rs12545263 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13251700 | 0.99[EUR][1000 genomes] |
rs13270234 | 0.97[EUR][1000 genomes] |
rs13271983 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13277538 | 0.91[ASN][1000 genomes] |
rs13280089 | 0.94[EUR][1000 genomes] |
rs1450127 | 0.84[ASN][1000 genomes] |
rs149992 | 0.81[ASN][1000 genomes] |
rs16914250 | 0.84[ASN][1000 genomes] |
rs16914376 | 0.91[ASN][1000 genomes] |
rs16914459 | 0.93[ASN][1000 genomes] |
rs17686196 | 0.89[EUR][1000 genomes] |
rs17758599 | 0.86[ASN][1000 genomes] |
rs1903311 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1906070 | 0.82[ASN][1000 genomes] |
rs203612 | 0.92[ASN][1000 genomes] |
rs203616 | 0.92[ASN][1000 genomes] |
rs203621 | 0.89[ASN][1000 genomes] |
rs203623 | 0.88[ASN][1000 genomes] |
rs203624 | 0.91[ASN][1000 genomes] |
rs203626 | 0.88[ASN][1000 genomes] |
rs203632 | 0.90[ASN][1000 genomes] |
rs203908 | 0.90[ASN][1000 genomes] |
rs203928 | 0.88[ASN][1000 genomes] |
rs203932 | 0.87[ASN][1000 genomes] |
rs203933 | 0.87[ASN][1000 genomes] |
rs203935 | 0.90[ASN][1000 genomes] |
rs203936 | 0.87[ASN][1000 genomes] |
rs203937 | 0.90[ASN][1000 genomes] |
rs203938 | 0.90[ASN][1000 genomes] |
rs203939 | 0.87[ASN][1000 genomes] |
rs203940 | 0.90[ASN][1000 genomes] |
rs203947 | 0.86[ASN][1000 genomes] |
rs203949 | 0.88[ASN][1000 genomes] |
rs203960 | 0.87[ASN][1000 genomes] |
rs2084590 | 0.84[ASN][1000 genomes] |
rs2084591 | 0.84[ASN][1000 genomes] |
rs2106156 | 0.90[EUR][1000 genomes] |
rs2157736 | 0.90[EUR][1000 genomes] |
rs34047312 | 0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34160877 | 0.80[EUR][1000 genomes] |
rs34641787 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34722367 | 0.91[ASN][1000 genomes] |
rs34908792 | 0.95[EUR][1000 genomes] |
rs34997857 | 0.93[ASN][1000 genomes] |
rs35093761 | 0.86[EUR][1000 genomes] |
rs35122483 | 0.90[EUR][1000 genomes] |
rs35418717 | 0.93[EUR][1000 genomes] |
rs35989044 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs36006902 | 0.91[ASN][1000 genomes] |
rs420489 | 0.92[ASN][1000 genomes] |
rs4873126 | 0.93[ASN][1000 genomes] |
rs4873127 | 0.93[ASN][1000 genomes] |
rs4873128 | 0.91[ASN][1000 genomes] |
rs4873129 | 0.91[ASN][1000 genomes] |
rs4873131 | 0.84[ASN][1000 genomes] |
rs4873132 | 0.84[ASN][1000 genomes] |
rs4873133 | 0.84[ASN][1000 genomes] |
rs4873134 | 0.84[ASN][1000 genomes] |
rs4873135 | 0.84[ASN][1000 genomes] |
rs4873405 | 0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4873406 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4873408 | 0.90[ASN][1000 genomes] |
rs4873412 | 0.90[ASN][1000 genomes] |
rs4873413 | 0.91[ASN][1000 genomes] |
rs4873414 | 0.91[ASN][1000 genomes] |
rs4873415 | 0.93[ASN][1000 genomes] |
rs4873416 | 0.91[ASN][1000 genomes] |
rs4873417 | 0.88[ASN][1000 genomes] |
rs4873418 | 0.91[ASN][1000 genomes] |
rs4873419 | 0.91[ASN][1000 genomes] |
rs4873420 | 0.91[ASN][1000 genomes] |
rs4873421 | 0.91[ASN][1000 genomes] |
rs4873426 | 0.84[ASN][1000 genomes] |
rs4873427 | 0.84[ASN][1000 genomes] |
rs4873428 | 0.84[ASN][1000 genomes] |
rs55889053 | 0.84[ASN][1000 genomes] |
rs56007637 | 0.93[ASN][1000 genomes] |
rs56413317 | 0.93[EUR][1000 genomes] |
rs56725 | 0.92[ASN][1000 genomes] |
rs62515375 | 0.87[ASN][1000 genomes] |
rs62516672 | 0.80[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs62516685 | 0.91[ASN][1000 genomes] |
rs62516686 | 0.94[EUR][1000 genomes] |
rs62516687 | 0.91[ASN][1000 genomes] |
rs6472947 | 0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs6983498 | 0.84[ASN][1000 genomes] |
rs6986896 | 0.88[ASN][1000 genomes] |
rs6988843 | 0.90[ASN][1000 genomes] |
rs6991753 | 0.88[ASN][1000 genomes] |
rs6996646 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7001686 | 0.88[ASN][1000 genomes] |
rs7002235 | 0.91[ASN][1000 genomes] |
rs7010037 | 0.91[ASN][1000 genomes] |
rs7013995 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7016161 | 0.91[ASN][1000 genomes] |
rs721441 | 0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7386487 | 0.88[ASN][1000 genomes] |
rs7817040 | 0.84[ASN][1000 genomes] |
rs7817638 | 0.84[ASN][1000 genomes] |
rs7820951 | 0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7824938 | 0.88[ASN][1000 genomes] |
rs7825053 | 0.88[ASN][1000 genomes] |
rs7825063 | 0.86[ASN][1000 genomes] |
rs7835849 | 0.84[ASN][1000 genomes] |
rs870754 | 0.93[ASN][1000 genomes] |
rs884561 | 0.91[ASN][1000 genomes] |
rs898520 | 0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3353749 | chr8:50530807-51139242 | Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv916392 | chr8:50827638-51395140 | Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759613 | chr8:50873293-51137995 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2758621 | chr8:50886593-51137995 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv6184 | chr8:50997525-51060432 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv539606 | chr8:51006600-51057478 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | esv1829361 | chr8:51021638-51101126 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv26 | chr8:51027781-51044881 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv1027998 | chr8:51032883-51084279 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
10 | nsv539607 | chr8:51032883-51084279 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:51032200-51046600 | Weak transcription | Fetal Brain Male | brain |
2 | chr8:51037800-51046800 | Weak transcription | Brain Germinal Matrix | brain |
3 | chr8:51038000-51047600 | Weak transcription | Right Atrium | heart |
4 | chr8:51040600-51048400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |