Variant report
Variant | rs73140581 |
---|---|
Chromosome Location | chr7:66633428-66633429 |
allele | A/G |
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] |
---|---|
rs10081302 | 0.82[ASN][1000 genomes] |
rs10081331 | 0.81[ASN][1000 genomes] |
rs10081381 | 0.81[ASN][1000 genomes] |
rs10155890 | 0.85[ASN][1000 genomes] |
rs10155918 | 0.91[ASN][1000 genomes] |
rs10155972 | 0.91[ASN][1000 genomes] |
rs10155983 | 0.88[ASN][1000 genomes] |
rs10156209 | 0.93[ASN][1000 genomes] |
rs10231586 | 0.88[ASN][1000 genomes] |
rs10234493 | 0.82[ASN][1000 genomes] |
rs10235588 | 0.93[ASN][1000 genomes] |
rs10243013 | 0.82[ASN][1000 genomes] |
rs10243217 | 0.93[ASN][1000 genomes] |
rs10243421 | 0.82[ASN][1000 genomes] |
rs10246747 | 0.88[ASN][1000 genomes] |
rs10250113 | 0.91[ASN][1000 genomes] |
rs10250487 | 0.93[ASN][1000 genomes] |
rs10251763 | 0.95[ASN][1000 genomes] |
rs10252143 | 0.95[ASN][1000 genomes] |
rs10253339 | 0.88[ASN][1000 genomes] |
rs10254788 | 0.82[ASN][1000 genomes] |
rs10256139 | 0.95[ASN][1000 genomes] |
rs10257949 | 0.95[ASN][1000 genomes] |
rs10262150 | 0.98[ASN][1000 genomes] |
rs10262781 | 0.87[ASN][1000 genomes] |
rs10267300 | 0.95[ASN][1000 genomes] |
rs10270292 | 0.86[ASN][1000 genomes] |
rs10272347 | 0.95[ASN][1000 genomes] |
rs10272591 | 0.95[ASN][1000 genomes] |
rs10274305 | 0.82[ASN][1000 genomes] |
rs10280699 | 0.89[ASN][1000 genomes] |
rs10950063 | 0.83[EUR][1000 genomes] |
rs11495955 | 0.89[AFR][1000 genomes] |
rs11760347 | 0.89[ASN][1000 genomes] |
rs11761100 | 0.89[ASN][1000 genomes] |
rs11764376 | 0.91[ASN][1000 genomes] |
rs11765001 | 0.89[AFR][1000 genomes] |
rs11767172 | 0.83[EUR][1000 genomes] |
rs11768286 | 0.89[AFR][1000 genomes] |
rs11770086 | 0.84[ASN][1000 genomes] |
rs11771408 | 0.80[ASN][1000 genomes] |
rs11772455 | 0.91[ASN][1000 genomes] |
rs11773012 | 0.86[ASN][1000 genomes] |
rs11773274 | 0.91[ASN][1000 genomes] |
rs11773730 | 0.91[ASN][1000 genomes] |
rs12154409 | 0.89[ASN][1000 genomes] |
rs12154419 | 0.91[ASN][1000 genomes] |
rs12155044 | 0.93[ASN][1000 genomes] |
rs12155051 | 0.95[ASN][1000 genomes] |
rs13225639 | 0.87[ASN][1000 genomes] |
rs13229085 | 0.87[ASN][1000 genomes] |
rs13233281 | 0.89[AFR][1000 genomes] |
rs13244997 | 0.82[ASN][1000 genomes] |
rs17139656 | 0.89[ASN][1000 genomes] |
rs1815098 | 0.86[ASN][1000 genomes] |
rs1815100 | 0.81[ASN][1000 genomes] |
rs1829931 | 0.81[ASN][1000 genomes] |
rs1880278 | 0.87[ASN][1000 genomes] |
rs1965480 | 0.86[ASN][1000 genomes] |
rs2421398 | 0.82[ASN][1000 genomes] |
rs2421404 | 0.91[ASN][1000 genomes] |
rs2421405 | 0.89[ASN][1000 genomes] |
rs2421419 | 0.93[ASN][1000 genomes] |
rs2690170 | 0.81[ASN][1000 genomes] |
rs28366417 | 0.95[ASN][1000 genomes] |
rs2844157 | 0.91[ASN][1000 genomes] |
rs2844170 | 0.81[ASN][1000 genomes] |
rs28534521 | 0.95[ASN][1000 genomes] |
rs28620117 | 0.87[ASN][1000 genomes] |
rs28651697 | 0.86[ASN][1000 genomes] |
rs28715521 | 0.93[ASN][1000 genomes] |
rs28888421 | 0.84[ASN][1000 genomes] |
rs2901424 | 0.82[ASN][1000 genomes] |
rs2901425 | 0.87[ASN][1000 genomes] |
rs3015884 | 0.91[ASN][1000 genomes] |
rs3107871 | 0.84[ASN][1000 genomes] |
rs34145691 | 0.95[ASN][1000 genomes] |
rs34146912 | 0.82[ASN][1000 genomes] |
rs34176733 | 0.82[ASN][1000 genomes] |
rs34317556 | 0.89[ASN][1000 genomes] |
rs34344363 | 0.86[ASN][1000 genomes] |
rs34654147 | 0.95[ASN][1000 genomes] |
rs35042775 | 0.88[ASN][1000 genomes] |
rs35048638 | 0.95[ASN][1000 genomes] |
rs35120837 | 0.82[ASN][1000 genomes] |
rs35290283 | 0.82[ASN][1000 genomes] |
rs35470341 | 0.87[ASN][1000 genomes] |
rs35723315 | 0.82[ASN][1000 genomes] |
rs35982871 | 0.82[ASN][1000 genomes] |
rs36108108 | 0.95[ASN][1000 genomes] |
rs3962076 | 0.95[ASN][1000 genomes] |
rs3980767 | 0.95[ASN][1000 genomes] |
rs3980775 | 0.91[ASN][1000 genomes] |
rs3980776 | 0.93[ASN][1000 genomes] |
rs3980778 | 0.84[ASN][1000 genomes] |
rs3980790 | 0.82[ASN][1000 genomes] |
rs4083135 | 0.87[ASN][1000 genomes] |
rs4101640 | 0.95[ASN][1000 genomes] |
rs4145350 | 0.91[ASN][1000 genomes] |
rs4295533 | 0.93[ASN][1000 genomes] |
rs4382353 | 0.86[ASN][1000 genomes] |
rs4433024 | 0.82[ASN][1000 genomes] |
rs4551224 | 0.95[ASN][1000 genomes] |
rs4552791 | 0.91[ASN][1000 genomes] |
rs4618581 | 0.95[ASN][1000 genomes] |
rs4621684 | 0.95[ASN][1000 genomes] |
rs4717353 | 0.95[ASN][1000 genomes] |
rs4718463 | 0.95[ASN][1000 genomes] |
rs4718464 | 0.91[ASN][1000 genomes] |
rs4718469 | 0.88[ASN][1000 genomes] |
rs4718470 | 0.98[ASN][1000 genomes] |
rs4718471 | 0.98[ASN][1000 genomes] |
rs4718501 | 0.80[ASN][1000 genomes] |
rs55756354 | 0.86[ASN][1000 genomes] |
rs55921608 | 0.80[ASN][1000 genomes] |
rs56001319 | 0.82[ASN][1000 genomes] |
rs61061833 | 0.84[ASN][1000 genomes] |
rs6460330 | 0.80[ASN][1000 genomes] |
rs67855845 | 0.95[ASN][1000 genomes] |
rs6952309 | 0.87[ASN][1000 genomes] |
rs6966142 | 0.87[ASN][1000 genomes] |
rs6972762 | 0.82[ASN][1000 genomes] |
rs6972777 | 0.82[ASN][1000 genomes] |
rs6978789 | 0.81[ASN][1000 genomes] |
rs6978918 | 0.80[ASN][1000 genomes] |
rs71535637 | 0.91[ASN][1000 genomes] |
rs71535638 | 0.93[ASN][1000 genomes] |
rs73134271 | 0.89[AFR][1000 genomes] |
rs73134299 | 0.89[AFR][1000 genomes] |
rs73136205 | 0.89[AFR][1000 genomes] |
rs73140561 | 0.89[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs73140602 | 0.95[ASN][1000 genomes] |
rs73142604 | 0.95[ASN][1000 genomes] |
rs7350002 | 0.82[ASN][1000 genomes] |
rs7350057 | 0.82[ASN][1000 genomes] |
rs7779596 | 0.81[ASN][1000 genomes] |
rs7780700 | 0.91[ASN][1000 genomes] |
rs7781804 | 0.91[ASN][1000 genomes] |
rs7783513 | 0.82[ASN][1000 genomes] |
rs7791642 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7792212 | 0.84[ASN][1000 genomes] |
rs7793101 | 0.84[ASN][1000 genomes] |
rs7793104 | 0.82[ASN][1000 genomes] |
rs7796133 | 0.84[ASN][1000 genomes] |
rs7804802 | 0.82[ASN][1000 genomes] |
rs9654771 | 0.95[ASN][1000 genomes] |
rs9654851 | 0.93[ASN][1000 genomes] |
rs9654853 | 0.95[ASN][1000 genomes] |
rs9654854 | 0.95[ASN][1000 genomes] |
rs9690120 | 0.87[ASN][1000 genomes] |
rs9690121 | 0.87[ASN][1000 genomes] |
rs9690145 | 0.87[ASN][1000 genomes] |
rs9690839 | 0.82[ASN][1000 genomes] |
rs9692192 | 0.82[ASN][1000 genomes] |
rs9692303 | 0.87[ASN][1000 genomes] |
rs9886204 | 0.82[ASN][1000 genomes] |
rs9886206 | 0.82[ASN][1000 genomes] |
rs9886263 | 0.82[ASN][1000 genomes] |
rs9886290 | 0.82[ASN][1000 genomes] |
rs9886306 | 0.82[ASN][1000 genomes] |
rs9886326 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758118 | chr7:66401430-66859253 | Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
2 | esv2759535 | chr7:66401430-66859253 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
3 | nsv888330 | chr7:66502171-66877880 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 39 gene(s) | inside rSNPs | diseases |
4 | nsv831019 | chr7:66516808-66720485 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 9 gene(s) | inside rSNPs | diseases |
5 | esv1802655 | chr7:66576034-66634666 | Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
6 | esv1816643 | chr7:66576034-66634666 | Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
7 | esv1840497 | chr7:66576034-66634666 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
8 | esv1851064 | chr7:66576034-66634666 | Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
9 | esv1832033 | chr7:66601324-66637001 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS | TF binding region | 1 gene(s) | inside rSNPs | diseases |
10 | esv1822512 | chr7:66613751-66637001 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS | n/a | n/a | inside rSNPs | diseases |
11 | esv1826252 | chr7:66613751-66637001 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS | n/a | n/a | inside rSNPs | diseases |
12 | esv1810114 | chr7:66621964-66636410 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription | n/a | n/a | inside rSNPs | diseases |
13 | esv2422035 | chr7:66621964-66676630 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
14 | esv1800770 | chr7:66629329-66645232 | Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | esv1831418 | chr7:66629329-66645232 | Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | esv1831706 | chr7:66629329-66645232 | Weak transcription Enhancers Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | nsv441983 | chr7:66629329-66645232 | Weak transcription Enhancers Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:66621600-66672000 | Weak transcription | Fetal Intestine Large | intestine |
2 | chr7:66628600-66684600 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
3 | chr7:66629000-66650200 | Weak transcription | Fetal Thymus | thymus |