Variant report
Variant | rs1737981 |
---|---|
Chromosome Location | chr1:192861690-192861691 |
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] |
---|---|
rs1070909 | 0.81[EUR][1000 genomes] |
rs1152746 | 0.82[EUR][1000 genomes] |
rs1231727 | 0.84[EUR][1000 genomes] |
rs1231729 | 0.81[EUR][1000 genomes] |
rs1231730 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231731 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231732 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231733 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231734 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231735 | 0.81[EUR][1000 genomes] |
rs1231736 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231737 | 0.84[EUR][1000 genomes] |
rs1231739 | 0.84[EUR][1000 genomes] |
rs1231740 | 0.84[EUR][1000 genomes] |
rs1231741 | 0.84[EUR][1000 genomes] |
rs1231742 | 0.84[EUR][1000 genomes] |
rs1231744 | 0.82[EUR][1000 genomes] |
rs1231746 | 0.83[EUR][1000 genomes] |
rs1231747 | 0.83[EUR][1000 genomes] |
rs1231749 | 0.83[EUR][1000 genomes] |
rs1231750 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1231751 | 0.83[EUR][1000 genomes] |
rs1231754 | 0.84[EUR][1000 genomes] |
rs1231757 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1231758 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1231762 | 0.82[EUR][1000 genomes] |
rs1231763 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231764 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231765 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1231766 | 0.82[EUR][1000 genomes] |
rs1231767 | 0.83[EUR][1000 genomes] |
rs1234722 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1237767 | 0.83[EUR][1000 genomes] |
rs12733094 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12756049 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12756953 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12757265 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs12758285 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs12758449 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1535034 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1620819 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1623376 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs16834948 | 0.85[EUR][1000 genomes] |
rs17524307 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs17524545 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs17590238 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1890973 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2473740 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2473741 | 0.82[EUR][1000 genomes] |
rs2473742 | 0.83[EUR][1000 genomes] |
rs2473744 | 0.81[EUR][1000 genomes] |
rs2473745 | 0.82[EUR][1000 genomes] |
rs2487284 | 0.82[EUR][1000 genomes] |
rs2487288 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2746068 | 0.83[EUR][1000 genomes] |
rs2797395 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs34120198 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs34424396 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs34562719 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs34732347 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs34838432 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs34867585 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs35040499 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs35471066 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs35845034 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs35879519 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs35997646 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs36005848 | 0.84[EUR][1000 genomes] |
rs4098556 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4332340 | 0.85[EUR][1000 genomes] |
rs4451535 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4658075 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs58739396 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs60382150 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs60756700 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6686024 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6692203 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs710142 | 0.82[EUR][1000 genomes] |
rs842922 | 0.84[EUR][1000 genomes] |
rs842923 | 0.84[EUR][1000 genomes] |
rs842924 | 0.83[EUR][1000 genomes] |
rs844529 | 0.83[EUR][1000 genomes] |
rs859888 | 0.83[EUR][1000 genomes] |
rs859890 | 0.84[EUR][1000 genomes] |
rs949982 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532618 | chr1:192537006-193149179 | Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 70 gene(s) | inside rSNPs | diseases |
2 | nsv548660 | chr1:192609268-192945348 | Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 22 gene(s) | inside rSNPs | diseases |
3 | esv3390055 | chr1:192859229-192863127 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
4 | esv3340601 | chr1:192859679-192862977 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
5 | esv3452627 | chr1:192860269-192862031 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
6 | esv3526514 | chr1:192860287-192862115 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
7 | esv3526511 | chr1:192860298-192862004 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
8 | esv3452625 | chr1:192860325-192861996 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
9 | esv3526513 | chr1:192860349-192861995 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
10 | esv3452626 | chr1:192860386-192861931 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
11 | esv3526512 | chr1:192860397-192861930 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
12 | esv3452628 | chr1:192860401-192861928 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
13 | esv3526515 | chr1:192860401-192861928 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
14 | esv1804510 | chr1:192860407-192861751 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
15 | esv1804742 | chr1:192860407-192861751 | Enhancers ZNF genes & repeats Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
16 | esv1805164 | chr1:192860407-192861751 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
17 | esv1806277 | chr1:192860407-192861751 | ZNF genes & repeats Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
18 | esv1809058 | chr1:192860407-192861751 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
19 | esv1809759 | chr1:192860407-192861751 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
20 | esv1811431 | chr1:192860407-192861751 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
21 | esv1811884 | chr1:192860407-192861751 | ZNF genes & repeats Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
22 | esv1829802 | chr1:192860407-192861751 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
23 | esv20998 | chr1:192860431-192861926 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:192843800-192861800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr1:192860600-192861800 | Weak transcription | Rectal Smooth Muscle | rectum |
3 | chr1:192860800-192862000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
4 | chr1:192860800-192862000 | Weak transcription | Colon Smooth Muscle | Colon |
5 | chr1:192860800-192863200 | Enhancers | HMEC | breast |