Variant report
Variant | rs4635847 |
---|---|
Chromosome Location | chr4:44993013-44993014 |
allele | C/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] |
---|---|
rs10000940 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10001739 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10003579 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10003776 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10003984 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10004173 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10006643 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10009882 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10031439 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10034588 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10433683 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10433684 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10938372 | 0.80[EUR][1000 genomes] |
rs10938378 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11723797 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11725423 | 0.80[ASN][1000 genomes] |
rs11726237 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11727488 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11730391 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11734842 | 0.88[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12501461 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12502784 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12503075 | 0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12504288 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12505440 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12509759 | 0.85[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12512128 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12512173 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12512921 | 0.99[ASN][1000 genomes] |
rs12513234 | 0.85[EUR][1000 genomes] |
rs13114174 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13123198 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13123623 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13125752 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13143643 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs13145245 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1390915 | 0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1390923 | 0.84[EUR][1000 genomes] |
rs1497000 | 0.81[EUR][1000 genomes] |
rs1497003 | 0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1948587 | 0.84[EUR][1000 genomes] |
rs28683174 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs28712193 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2882027 | 0.83[EUR][1000 genomes] |
rs34298665 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs34398887 | 0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs34625281 | 0.83[EUR][1000 genomes] |
rs34725881 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs34771773 | 0.89[ASN][1000 genomes] |
rs35739449 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4264865 | 0.81[EUR][1000 genomes] |
rs4267770 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4280774 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4312794 | 0.88[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4377625 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4410559 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4431264 | 0.82[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4447894 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4456993 | 0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4464602 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4467605 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4481265 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4492035 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4505863 | 0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4558900 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4560452 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4571371 | 0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4580687 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4621472 | 0.84[AFR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4629490 | 0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4632690 | 0.86[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4639112 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4695069 | 0.88[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4695070 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs5002959 | 0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62409744 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62411580 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62411584 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6447395 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6447396 | 0.99[ASN][1000 genomes] |
rs6447397 | 0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6447398 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6447399 | 0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6447400 | 0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6447401 | 0.92[ASN][1000 genomes] |
rs6447402 | 0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6820860 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6822744 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6823446 | 0.87[EUR][1000 genomes] |
rs6823641 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6828498 | 0.85[EUR][1000 genomes] |
rs6832190 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6839710 | 0.96[ASN][1000 genomes] |
rs6848088 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6848089 | 0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6848542 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6855537 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7655634 | 0.81[EUR][1000 genomes] |
rs7657077 | 0.81[EUR][1000 genomes] |
rs7658399 | 0.81[EUR][1000 genomes] |
rs7677319 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7678059 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7679461 | 0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7682854 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7698277 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7699473 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531944 | chr4:44299343-45200700 | Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
2 | nsv1014327 | chr4:44735209-45218149 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv878979 | chr4:44871931-45102488 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv432591 | chr4:44922068-45017576 | Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv432592 | chr4:44932439-45005872 | Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
6 | nsv432594 | chr4:44932945-45033572 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv1014721 | chr4:44950223-44999607 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
8 | nsv432595 | chr4:44951672-45010972 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
9 | nsv432596 | chr4:44951672-45037672 | Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
10 | nsv594098 | chr4:44955950-45004987 | Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
11 | nsv594099 | chr4:44955964-45004987 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
12 | nsv1004138 | chr4:44956309-45006323 | Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
13 | esv2757056 | chr4:44960444-45033572 | Enhancers Weak transcription ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
14 | esv2759250 | chr4:44960444-45033572 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
15 | nsv594100 | chr4:44961533-45004987 | Enhancers ZNF genes & repeats Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
16 | nsv878980 | chr4:44961533-45015525 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
17 | nsv878981 | chr4:44961533-45018583 | Enhancers ZNF genes & repeats Weak transcription Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
18 | esv2763861 | chr4:44964479-45011262 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
19 | nsv1005919 | chr4:44965184-45006323 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
20 | nsv10488 | chr4:44965278-45011616 | Enhancers Strong transcription Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
21 | nsv1006132 | chr4:44967004-44999607 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
22 | nsv1004845 | chr4:44967004-45005852 | Weak transcription Strong transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
23 | nsv1007329 | chr4:44967004-45006180 | Enhancers Strong transcription Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
24 | nsv1009747 | chr4:44967004-45006323 | Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
25 | nsv1013463 | chr4:44967004-45013835 | Enhancers Weak transcription Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
26 | nsv1005572 | chr4:44967004-45017576 | Enhancers Weak transcription Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
27 | nsv1013324 | chr4:44968495-44999607 | Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
28 | nsv998011 | chr4:44968495-45006180 | Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
29 | nsv1005217 | chr4:44968495-45006323 | Enhancers Strong transcription Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
30 | esv34200 | chr4:44968572-45005872 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
31 | esv34309 | chr4:44968572-45005872 | Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
32 | esv2752046 | chr4:44968572-45005872 | Enhancers Strong transcription Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
33 | nsv432599 | chr4:44968572-45005872 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
34 | nsv432597 | chr4:44968572-45010972 | Enhancers Weak transcription Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
35 | esv2752047 | chr4:44968572-45072206 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
36 | nsv516124 | chr4:44968603-44998994 | Strong transcription Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
37 | esv2830137 | chr4:44968603-45004987 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
38 | nsv594101 | chr4:44968603-45004987 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
39 | nsv594102 | chr4:44968603-45007208 | Weak transcription Enhancers Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
40 | nsv1002121 | chr4:44969388-45006323 | Strong transcription Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
41 | esv34407 | chr4:44970482-45005852 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
42 | esv2752048 | chr4:44970482-45005872 | Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
43 | nsv1001880 | chr4:44970482-45006323 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
44 | nsv1008257 | chr4:44973414-44999607 | Enhancers Strong transcription Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
45 | nsv594103 | chr4:44982938-45004987 | Enhancers Strong transcription Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
46 | nsv878982 | chr4:44982938-45031256 | Enhancers Weak transcription Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
47 | nsv878983 | chr4:44982938-45039597 | Enhancers Weak transcription Flanking Active TSS Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
48 | esv1830314 | chr4:44983899-45023201 | Enhancers Weak transcription Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
49 | nsv1001539 | chr4:44991475-45006323 | Enhancers Weak transcription Strong transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:44988600-44993400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |