Variant report
Variant | rs1159715 |
---|---|
Chromosome Location | chr4:69807404-69807405 |
allele | A/C |
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] |
---|---|
rs10000598 | 0.83[EUR][1000 genomes] |
rs10001065 | 0.90[EUR][1000 genomes] |
rs10006282 | 0.83[EUR][1000 genomes] |
rs10010699 | 0.83[EUR][1000 genomes] |
rs10013724 | 0.90[EUR][1000 genomes] |
rs10024664 | 0.90[EUR][1000 genomes] |
rs10032748 | 0.89[EUR][1000 genomes] |
rs1020767 | 0.86[EUR][1000 genomes] |
rs10518057 | 0.83[EUR][1000 genomes] |
rs10903220 | 0.90[EUR][1000 genomes] |
rs10903221 | 0.90[EUR][1000 genomes] |
rs10903224 | 0.83[EUR][1000 genomes] |
rs11249512 | 0.92[EUR][1000 genomes] |
rs11249513 | 0.92[EUR][1000 genomes] |
rs11249515 | 0.92[EUR][1000 genomes] |
rs1159714 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11736796 | 0.89[EUR][1000 genomes] |
rs11932983 | 0.81[EUR][1000 genomes] |
rs11936412 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11940320 | 0.87[EUR][1000 genomes] |
rs11946857 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11946976 | 0.81[EUR][1000 genomes] |
rs12499093 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12500933 | 0.85[EUR][1000 genomes] |
rs12508920 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12509040 | 0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12509066 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12510036 | 0.87[EUR][1000 genomes] |
rs13104293 | 0.85[EUR][1000 genomes] |
rs13106664 | 0.90[EUR][1000 genomes] |
rs13113544 | 0.84[EUR][1000 genomes] |
rs13128286 | 0.89[EUR][1000 genomes] |
rs13128843 | 0.90[EUR][1000 genomes] |
rs13132528 | 0.83[EUR][1000 genomes] |
rs13148179 | 0.85[EUR][1000 genomes] |
rs13148603 | 0.83[EUR][1000 genomes] |
rs1379813 | 0.83[EUR][1000 genomes] |
rs1379816 | 0.83[EUR][1000 genomes] |
rs1458236 | 0.89[EUR][1000 genomes] |
rs1458237 | 0.89[EUR][1000 genomes] |
rs1458242 | 0.87[EUR][1000 genomes] |
rs1458243 | 0.82[EUR][1000 genomes] |
rs1458245 | 0.83[EUR][1000 genomes] |
rs1458246 | 0.83[EUR][1000 genomes] |
rs1598904 | 0.83[EUR][1000 genomes] |
rs17146967 | 0.85[EUR][1000 genomes] |
rs17605102 | 0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1841037 | 0.85[EUR][1000 genomes] |
rs1902925 | 0.90[EUR][1000 genomes] |
rs1902926 | 0.90[EUR][1000 genomes] |
rs1902927 | 0.90[EUR][1000 genomes] |
rs1902928 | 0.90[EUR][1000 genomes] |
rs1962953 | 0.90[EUR][1000 genomes] |
rs1968764 | 0.82[EUR][1000 genomes] |
rs1989329 | 0.80[EUR][1000 genomes] |
rs1993546 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1993547 | 0.84[EUR][1000 genomes] |
rs2009312 | 0.90[EUR][1000 genomes] |
rs2017125 | 0.90[EUR][1000 genomes] |
rs2018150 | 0.90[EUR][1000 genomes] |
rs2125305 | 0.90[EUR][1000 genomes] |
rs2168840 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2168841 | 0.92[EUR][1000 genomes] |
rs2331561 | 0.92[EUR][1000 genomes] |
rs2331562 | 0.92[EUR][1000 genomes] |
rs2331577 | 0.89[EUR][1000 genomes] |
rs3088249 | 0.90[EUR][1000 genomes] |
rs3749511 | 0.89[EUR][1000 genomes] |
rs3749513 | 0.90[EUR][1000 genomes] |
rs3828504 | 0.89[EUR][1000 genomes] |
rs4412056 | 0.89[EUR][1000 genomes] |
rs4518317 | 0.90[EUR][1000 genomes] |
rs4694358 | 0.86[EUR][1000 genomes] |
rs4694389 | 0.85[EUR][1000 genomes] |
rs4694448 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4694449 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55647928 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs55795005 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs55831171 | 0.81[EUR][1000 genomes] |
rs56371633 | 0.85[EUR][1000 genomes] |
rs56943005 | 0.81[EUR][1000 genomes] |
rs60276248 | 0.81[EUR][1000 genomes] |
rs6600857 | 0.90[EUR][1000 genomes] |
rs6842605 | 0.85[EUR][1000 genomes] |
rs6843537 | 0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6843550 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6847539 | 0.91[EUR][1000 genomes] |
rs6849125 | 0.87[EUR][1000 genomes] |
rs6858791 | 0.82[EUR][1000 genomes] |
rs7441753 | 0.83[EUR][1000 genomes] |
rs7666446 | 0.90[EUR][1000 genomes] |
rs7674475 | 0.90[EUR][1000 genomes] |
rs7692753 | 0.84[EUR][1000 genomes] |
rs9329037 | 0.82[EUR][1000 genomes] |
rs969338 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs994229 | 0.90[EUR][1000 genomes] |
rs9996467 | 0.90[EUR][1000 genomes] |
rs9999996 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1005513 | chr4:69446718-69890307 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
2 | nsv999654 | chr4:69661415-70132110 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
3 | esv3420586 | chr4:69680878-70322918 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 41 gene(s) | inside rSNPs | diseases |
4 | esv3398036 | chr4:69700493-69841391 | Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
5 | nsv1067773 | chr4:69718248-70715727 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
6 | esv3468151 | chr4:69718675-70322776 | Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
7 | esv3468153 | chr4:69718675-70322776 | Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
8 | nsv436447 | chr4:69743339-69851390 | Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
9 | nsv4372 | chr4:69764499-69810115 | Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
10 | nsv967758 | chr4:69780530-69870183 | Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
11 | nsv829962 | chr4:69786869-69910283 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
12 | esv3430337 | chr4:69807263-69809311 | Strong transcription Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:69792400-69812600 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
2 | chr4:69794600-69809400 | Weak transcription | Pancreas | Pancrea |
3 | chr4:69796400-69814400 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
4 | chr4:69796600-69813800 | Weak transcription | Liver | Liver |
5 | chr4:69804400-69809400 | Weak transcription | HepG2 | liver |
6 | chr4:69806000-69809400 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
7 | chr4:69807000-69812600 | Weak transcription | Fetal Intestine Small | intestine |
8 | chr4:69807400-69809200 | Weak transcription | Fetal Intestine Large | intestine |
9 | chr4:69807400-69812200 | Weak transcription | Duodenum Mucosa | Duodenum |