Variant report
Variant | rs13256139 |
---|---|
Chromosome Location | chr8:46918722-46918723 |
allele | A/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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10090166 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10095720 | 0.84[AMR][1000 genomes] |
rs10216494 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10216568 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10216759 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10866884 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs10866903 | 0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11136096 | 0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11136124 | 0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11136130 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11136135 | 0.81[AMR][1000 genomes] |
rs11136181 | 0.81[AMR][1000 genomes] |
rs11136210 | 0.88[AMR][1000 genomes] |
rs11136213 | 0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11136214 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11136247 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11136249 | 0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11776629 | 0.87[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs11776913 | 0.86[AMR][1000 genomes] |
rs11778237 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11779562 | 0.93[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11782164 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11783264 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11785812 | 0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12543537 | 0.84[AMR][1000 genomes] |
rs12544729 | 0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12545363 | 0.85[AMR][1000 genomes] |
rs12545614 | 0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12676202 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12678280 | 0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12678943 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12678983 | 0.88[AMR][1000 genomes] |
rs12679978 | 0.88[AMR][1000 genomes] |
rs12680749 | 0.88[AMR][1000 genomes] |
rs12681258 | 0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13249362 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13253473 | 0.83[AMR][1000 genomes] |
rs13253742 | 0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs13254856 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13255141 | 0.94[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13257202 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13261801 | 0.94[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13262569 | 0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13264613 | 0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13267299 | 0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13267310 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13267636 | 0.94[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13270532 | 0.83[AMR][1000 genomes] |
rs13272118 | 0.91[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13275242 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13278440 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1404489 | 0.81[AMR][1000 genomes] |
rs1404490 | 0.82[AMR][1000 genomes] |
rs1524898 | 0.81[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs1587137 | 0.87[AMR][1000 genomes] |
rs1608733 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1880503 | 0.82[AMR][1000 genomes] |
rs1880505 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1880507 | 0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1880508 | 0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1917427 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1917428 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1917435 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1917436 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1917437 | 0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2177671 | 0.94[AMR][1000 genomes] |
rs2204395 | 0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4242437 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4265202 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4349992 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4475488 | 0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4486212 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4509329 | 0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4872560 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4872565 | 0.82[AMR][1000 genomes] |
rs4872731 | 0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4872732 | 0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4872742 | 0.91[AMR][1000 genomes] |
rs7005506 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7016563 | 0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72638649 | 0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7293738 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7816964 | 0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7819716 | 0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs9650434 | 0.84[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1031442 | chr8:46847522-46927075 | ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
2 | nsv1018446 | chr8:46847522-46933024 | Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
3 | nsv1034986 | chr8:46847522-46936604 | ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
4 | nsv1033056 | chr8:46847522-46954695 | Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription | Chromatin interactive region | 4 gene(s) | inside rSNPs | n/a |
5 | nsv1017900 | chr8:46847522-47024380 | ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1028273 | chr8:46847522-47063432 | ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
7 | nsv1022441 | chr8:46847522-47175405 | ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
8 | nsv1020385 | chr8:46847522-47199227 | ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
9 | nsv1026941 | chr8:46847522-47203990 | Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
10 | nsv1031996 | chr8:46847522-47361594 | ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
11 | nsv1018413 | chr8:46847522-47436605 | ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
12 | nsv1030943 | chr8:46847522-47517000 | Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
13 | nsv1031244 | chr8:46847522-47735165 | ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
14 | nsv1032451 | chr8:46847522-47743250 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
15 | nsv1018479 | chr8:46847522-47776897 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
16 | esv2761184 | chr8:46847534-47743262 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
17 | nsv428199 | chr8:46868542-47280620 | Genic enhancers ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
18 | esv2829896 | chr8:46896972-47287147 | ZNF genes & repeats Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
19 | nsv611229 | chr8:46902917-47439358 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
20 | nsv1034366 | chr8:46912015-47024380 | ZNF genes & repeats Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
21 | nsv1015309 | chr8:46912015-47175405 | ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:46917400-46919600 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
2 | chr8:46917800-46919200 | ZNF genes & repeats | Liver | Liver |