Variant report
Variant | rs3105358 |
---|---|
Chromosome Location | chr10:58888848-58888849 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:58887742..58890502-chr10:58913371..58916213,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10763457 | 0.83[ASN][1000 genomes] |
rs10825986 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10825987 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10825988 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10825989 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10825990 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10825991 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10825992 | 0.83[ASN][1000 genomes] |
rs10825993 | 0.83[ASN][1000 genomes] |
rs10825994 | 0.83[ASN][1000 genomes] |
rs11005639 | 0.88[ASN][1000 genomes] |
rs11005651 | 0.88[ASN][1000 genomes] |
rs11005687 | 0.94[ASN][1000 genomes] |
rs1116023 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1116024 | 0.84[EUR][1000 genomes] |
rs1116026 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1120047 | 0.95[ASN][1000 genomes] |
rs11817223 | 0.94[ASN][1000 genomes] |
rs12240722 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12240853 | 0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12242643 | 0.82[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12262585 | 0.82[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12268403 | 0.81[ASN][1000 genomes] |
rs12269721 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1303961 | 0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1394103 | 0.88[ASN][1000 genomes] |
rs1503903 | 0.81[EUR][1000 genomes] |
rs1503904 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1503905 | 0.88[ASN][1000 genomes] |
rs1503906 | 0.88[ASN][1000 genomes] |
rs1503907 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1503908 | 0.88[ASN][1000 genomes] |
rs1503911 | 0.88[ASN][1000 genomes] |
rs1503914 | 0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs16910232 | 0.88[ASN][1000 genomes] |
rs16910285 | 0.94[ASN][1000 genomes] |
rs1818173 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1827580 | 0.88[ASN][1000 genomes] |
rs1875769 | 0.88[ASN][1000 genomes] |
rs1875770 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1875771 | 0.88[ASN][1000 genomes] |
rs1875773 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1910496 | 0.88[ASN][1000 genomes] |
rs1915690 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1915691 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1960403 | 0.84[EUR][1000 genomes] |
rs2007334 | 0.88[ASN][1000 genomes] |
rs2013953 | 0.88[ASN][1000 genomes] |
rs2013958 | 0.88[ASN][1000 genomes] |
rs2036504 | 0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2036510 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2055556 | 0.88[ASN][1000 genomes] |
rs2102229 | 0.88[ASN][1000 genomes] |
rs2102230 | 0.85[ASN][1000 genomes] |
rs2174231 | 0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2174232 | 0.94[ASN][1000 genomes] |
rs2202301 | 0.88[ASN][1000 genomes] |
rs2893720 | 0.88[ASN][1000 genomes] |
rs3104619 | 1.00[ASN][1000 genomes] |
rs3104620 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3104621 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3104622 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3104623 | 0.88[ASN][1000 genomes] |
rs3104624 | 0.83[EUR][1000 genomes] |
rs3104626 | 0.88[ASN][1000 genomes] |
rs3104627 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3104628 | 0.88[ASN][1000 genomes] |
rs3104629 | 0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3104633 | 0.88[ASN][1000 genomes] |
rs3104634 | 0.88[ASN][1000 genomes] |
rs3104635 | 0.80[ASN][1000 genomes] |
rs3104636 | 0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3104669 | 0.87[EUR][1000 genomes] |
rs3104670 | 0.87[EUR][1000 genomes] |
rs3104671 | 0.95[ASN][1000 genomes] |
rs3104672 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3104673 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3104676 | 0.98[ASN][1000 genomes] |
rs3104677 | 1.00[ASN][1000 genomes] |
rs3104678 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3105300 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3105301 | 0.88[ASN][1000 genomes] |
rs3105303 | 0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3105306 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3105307 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs3105308 | 0.88[ASN][1000 genomes] |
rs3105309 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3105310 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3105314 | 0.88[ASN][1000 genomes] |
rs3105316 | 0.88[ASN][1000 genomes] |
rs3105321 | 0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3105349 | 0.98[ASN][1000 genomes] |
rs3105350 | 0.98[ASN][1000 genomes] |
rs3105353 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3105354 | 1.00[ASN][1000 genomes] |
rs3105355 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3105356 | 0.88[ASN][1000 genomes] |
rs3105357 | 1.00[ASN][1000 genomes] |
rs3107504 | 0.94[ASN][1000 genomes] |
rs3107511 | 0.94[ASN][1000 genomes] |
rs34384617 | 0.91[ASN][1000 genomes] |
rs35642791 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs35674272 | 0.83[ASN][1000 genomes] |
rs3861043 | 0.85[ASN][1000 genomes] |
rs4347303 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4935688 | 0.94[ASN][1000 genomes] |
rs4935689 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6481256 | 0.84[EUR][1000 genomes] |
rs6481257 | 0.84[EUR][1000 genomes] |
rs6481258 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6481259 | 0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7068379 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7075131 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7076261 | 0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7080973 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7081958 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7083057 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7089308 | 0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7094185 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7097836 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs71020944 | 0.88[ASN][1000 genomes] |
rs7909495 | 0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7912607 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7915950 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs924792 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs924794 | 0.88[ASN][1000 genomes] |
rs983569 | 0.88[ASN][1000 genomes] |
rs983570 | 0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs988162 | 0.89[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs988486 | 0.88[ASN][1000 genomes] |
rs990279 | 0.88[ASN][1000 genomes] |
rs995236 | 0.88[ASN][1000 genomes] |
rs995237 | 0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv895513 | chr10:58672533-58979792 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv895515 | chr10:58802422-58913651 | Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | esv2757391 | chr10:58822244-58948207 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2759759 | chr10:58822244-58948207 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv895517 | chr10:58836950-58957774 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv895519 | chr10:58843951-58905847 | Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv895520 | chr10:58843951-58933549 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv551106 | chr10:58846575-58892275 | ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | esv2756345 | chr10:58846594-59027194 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv895521 | chr10:58849853-58963458 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
11 | esv2829927 | chr10:58849853-58979792 | Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | nsv551107 | chr10:58853784-58918899 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
13 | nsv895522 | chr10:58853784-58918899 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
14 | nsv895523 | chr10:58853784-58945720 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
15 | nsv895524 | chr10:58853784-58953960 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
16 | nsv895525 | chr10:58853784-58963458 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
17 | nsv895526 | chr10:58853784-58970006 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
18 | nsv895527 | chr10:58853784-58979792 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
19 | nsv895528 | chr10:58853784-58991581 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
20 | nsv551108 | chr10:58870687-58918899 | Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
21 | esv34583 | chr10:58883172-58936909 | Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
22 | esv2754933 | chr10:58883172-58936909 | Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
23 | esv2753099 | chr10:58883172-58948207 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv467280 | chr10:58885646-58936553 | Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
25 | nsv551109 | chr10:58885646-58936553 | Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
26 | nsv895529 | chr10:58885646-58936553 | Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
27 | nsv895530 | chr10:58885646-58937708 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
28 | nsv895531 | chr10:58885646-58938552 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:58886600-58897200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |