Variant report
Variant | rs61957978 |
---|---|
Chromosome Location | chr13:52924249-52924250 |
allele | C/T |
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] |
---|---|
rs1053245 | 1.00[ASN][1000 genomes] |
rs11148250 | 1.00[ASN][1000 genomes] |
rs11148251 | 1.00[ASN][1000 genomes] |
rs12184815 | 0.87[ASN][1000 genomes] |
rs17087405 | 1.00[ASN][1000 genomes] |
rs28589286 | 1.00[ASN][1000 genomes] |
rs28756262 | 1.00[ASN][1000 genomes] |
rs34355831 | 1.00[ASN][1000 genomes] |
rs35975899 | 1.00[ASN][1000 genomes] |
rs41292810 | 1.00[ASN][1000 genomes] |
rs41292818 | 1.00[ASN][1000 genomes] |
rs55850688 | 1.00[ASN][1000 genomes] |
rs56173235 | 1.00[ASN][1000 genomes] |
rs56249382 | 1.00[ASN][1000 genomes] |
rs57412438 | 1.00[ASN][1000 genomes] |
rs57831032 | 1.00[ASN][1000 genomes] |
rs57904860 | 1.00[ASN][1000 genomes] |
rs58655347 | 1.00[ASN][1000 genomes] |
rs60322427 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60406129 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61011708 | 1.00[ASN][1000 genomes] |
rs61171418 | 1.00[ASN][1000 genomes] |
rs61677410 | 1.00[ASN][1000 genomes] |
rs61957307 | 1.00[ASN][1000 genomes] |
rs61957966 | 0.87[ASN][1000 genomes] |
rs61957967 | 1.00[ASN][1000 genomes] |
rs61957976 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61957977 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61957980 | 1.00[ASN][1000 genomes] |
rs61957981 | 1.00[ASN][1000 genomes] |
rs61957982 | 1.00[ASN][1000 genomes] |
rs61957983 | 1.00[ASN][1000 genomes] |
rs61957984 | 1.00[ASN][1000 genomes] |
rs61957986 | 1.00[ASN][1000 genomes] |
rs61957987 | 1.00[ASN][1000 genomes] |
rs61957988 | 1.00[ASN][1000 genomes] |
rs61957989 | 1.00[ASN][1000 genomes] |
rs61957993 | 1.00[ASN][1000 genomes] |
rs61957995 | 1.00[ASN][1000 genomes] |
rs61957996 | 1.00[ASN][1000 genomes] |
rs61957997 | 1.00[ASN][1000 genomes] |
rs61958009 | 1.00[ASN][1000 genomes] |
rs61958010 | 1.00[ASN][1000 genomes] |
rs61958011 | 1.00[ASN][1000 genomes] |
rs61958012 | 1.00[ASN][1000 genomes] |
rs61958013 | 1.00[ASN][1000 genomes] |
rs61958014 | 1.00[ASN][1000 genomes] |
rs61958016 | 1.00[ASN][1000 genomes] |
rs61958017 | 1.00[ASN][1000 genomes] |
rs61958018 | 1.00[ASN][1000 genomes] |
rs61958019 | 1.00[ASN][1000 genomes] |
rs61958020 | 1.00[ASN][1000 genomes] |
rs61958023 | 1.00[ASN][1000 genomes] |
rs61958024 | 1.00[ASN][1000 genomes] |
rs61958026 | 1.00[ASN][1000 genomes] |
rs61958048 | 1.00[ASN][1000 genomes] |
rs61958049 | 1.00[ASN][1000 genomes] |
rs61958051 | 1.00[ASN][1000 genomes] |
rs61958052 | 1.00[ASN][1000 genomes] |
rs61958053 | 1.00[ASN][1000 genomes] |
rs61958055 | 1.00[ASN][1000 genomes] |
rs61958057 | 1.00[ASN][1000 genomes] |
rs61958058 | 1.00[ASN][1000 genomes] |
rs61958059 | 1.00[ASN][1000 genomes] |
rs61959660 | 1.00[ASN][1000 genomes] |
rs61959661 | 1.00[ASN][1000 genomes] |
rs61959663 | 1.00[ASN][1000 genomes] |
rs61959664 | 1.00[ASN][1000 genomes] |
rs61959666 | 1.00[ASN][1000 genomes] |
rs61959667 | 1.00[ASN][1000 genomes] |
rs61959668 | 1.00[ASN][1000 genomes] |
rs61959669 | 1.00[ASN][1000 genomes] |
rs61959670 | 1.00[ASN][1000 genomes] |
rs61959672 | 1.00[ASN][1000 genomes] |
rs61959673 | 1.00[ASN][1000 genomes] |
rs61959674 | 1.00[ASN][1000 genomes] |
rs61959675 | 1.00[ASN][1000 genomes] |
rs61959676 | 1.00[ASN][1000 genomes] |
rs61959677 | 1.00[ASN][1000 genomes] |
rs61959679 | 1.00[ASN][1000 genomes] |
rs61959698 | 1.00[ASN][1000 genomes] |
rs61959702 | 1.00[ASN][1000 genomes] |
rs61959706 | 1.00[ASN][1000 genomes] |
rs61959707 | 1.00[ASN][1000 genomes] |
rs61959784 | 1.00[ASN][1000 genomes] |
rs7321936 | 0.84[EUR][1000 genomes] |
rs7331858 | 0.84[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7983047 | 1.00[ASN][1000 genomes] |
rs9526881 | 0.86[ASN][1000 genomes] |
rs9526882 | 1.00[ASN][1000 genomes] |
rs9526888 | 1.00[ASN][1000 genomes] |
rs9526890 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9526891 | 0.83[AMR][1000 genomes] |
rs9526892 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9526895 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9526896 | 1.00[ASN][1000 genomes] |
rs9526897 | 1.00[ASN][1000 genomes] |
rs9526898 | 1.00[ASN][1000 genomes] |
rs9526901 | 1.00[ASN][1000 genomes] |
rs9526902 | 1.00[ASN][1000 genomes] |
rs9526903 | 1.00[ASN][1000 genomes] |
rs9526905 | 0.86[ASN][1000 genomes] |
rs9526906 | 1.00[ASN][1000 genomes] |
rs9526908 | 1.00[ASN][1000 genomes] |
rs9526909 | 1.00[ASN][1000 genomes] |
rs9526910 | 1.00[ASN][1000 genomes] |
rs9526915 | 1.00[ASN][1000 genomes] |
rs9526916 | 1.00[ASN][1000 genomes] |
rs9526924 | 1.00[ASN][1000 genomes] |
rs9526926 | 1.00[ASN][1000 genomes] |
rs9535975 | 1.00[ASN][1000 genomes] |
rs9535991 | 0.86[ASN][1000 genomes] |
rs9536003 | 0.87[ASN][1000 genomes] |
rs9536004 | 1.00[ASN][1000 genomes] |
rs9536005 | 1.00[ASN][1000 genomes] |
rs9536007 | 0.86[ASN][1000 genomes] |
rs9536008 | 1.00[ASN][1000 genomes] |
rs9536009 | 1.00[ASN][1000 genomes] |
rs9536018 | 1.00[ASN][1000 genomes] |
rs9536019 | 1.00[ASN][1000 genomes] |
rs9536020 | 1.00[ASN][1000 genomes] |
rs9536022 | 1.00[ASN][1000 genomes] |
rs9536023 | 1.00[ASN][1000 genomes] |
rs9536025 | 1.00[ASN][1000 genomes] |
rs9536026 | 1.00[ASN][1000 genomes] |
rs9536027 | 1.00[ASN][1000 genomes] |
rs9536028 | 1.00[ASN][1000 genomes] |
rs9536029 | 1.00[ASN][1000 genomes] |
rs9536031 | 1.00[ASN][1000 genomes] |
rs9536033 | 1.00[ASN][1000 genomes] |
rs9536034 | 1.00[ASN][1000 genomes] |
rs9536036 | 1.00[ASN][1000 genomes] |
rs9536037 | 1.00[ASN][1000 genomes] |
rs9536038 | 1.00[ASN][1000 genomes] |
rs9536040 | 1.00[ASN][1000 genomes] |
rs9536041 | 1.00[ASN][1000 genomes] |
rs9536042 | 1.00[ASN][1000 genomes] |
rs9536043 | 1.00[ASN][1000 genomes] |
rs9536044 | 0.86[ASN][1000 genomes] |
rs9536047 | 1.00[ASN][1000 genomes] |
rs9536049 | 1.00[ASN][1000 genomes] |
rs9536050 | 1.00[ASN][1000 genomes] |
rs9536051 | 1.00[ASN][1000 genomes] |
rs9536053 | 1.00[ASN][1000 genomes] |
rs9536054 | 1.00[ASN][1000 genomes] |
rs9536056 | 1.00[ASN][1000 genomes] |
rs9536057 | 1.00[ASN][1000 genomes] |
rs9536058 | 1.00[ASN][1000 genomes] |
rs9536059 | 1.00[ASN][1000 genomes] |
rs9536060 | 1.00[ASN][1000 genomes] |
rs9536061 | 1.00[ASN][1000 genomes] |
rs9536062 | 1.00[ASN][1000 genomes] |
rs9536063 | 1.00[ASN][1000 genomes] |
rs9536064 | 1.00[ASN][1000 genomes] |
rs9536065 | 1.00[ASN][1000 genomes] |
rs9536067 | 1.00[ASN][1000 genomes] |
rs9536068 | 1.00[ASN][1000 genomes] |
rs9536070 | 1.00[ASN][1000 genomes] |
rs9536072 | 1.00[ASN][1000 genomes] |
rs9536073 | 1.00[ASN][1000 genomes] |
rs9536074 | 1.00[ASN][1000 genomes] |
rs9536075 | 1.00[ASN][1000 genomes] |
rs9536076 | 1.00[ASN][1000 genomes] |
rs9536077 | 1.00[ASN][1000 genomes] |
rs9536078 | 1.00[ASN][1000 genomes] |
rs9536080 | 1.00[ASN][1000 genomes] |
rs9536081 | 1.00[ASN][1000 genomes] |
rs9536083 | 1.00[ASN][1000 genomes] |
rs9536084 | 1.00[ASN][1000 genomes] |
rs9536085 | 1.00[ASN][1000 genomes] |
rs9536087 | 1.00[ASN][1000 genomes] |
rs9536088 | 1.00[ASN][1000 genomes] |
rs9596645 | 1.00[ASN][1000 genomes] |
rs9741870 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv934070 | chr13:52362588-53174923 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 59 gene(s) | inside rSNPs | diseases |
2 | nsv1040931 | chr13:52564792-53350914 | Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 54 gene(s) | inside rSNPs | diseases |
3 | nsv541773 | chr13:52564792-53350914 | Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 54 gene(s) | inside rSNPs | diseases |
4 | nsv428288 | chr13:52728370-53068132 | Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
5 | nsv819887 | chr13:52772113-52926921 | Enhancers Active TSS Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
6 | nsv900084 | chr13:52835231-53119704 | Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
7 | nsv977385 | chr13:52918841-52936623 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:52918800-52924400 | Enhancers | HMEC | breast |
2 | chr13:52920000-52924400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr13:52921600-52924400 | Enhancers | Cortex derived primary cultured neurospheres | brain |
4 | chr13:52921600-52924400 | Enhancers | Osteobl | bone |
5 | chr13:52922200-52924400 | Enhancers | Muscle Satellite Cultured Cells | -- |
6 | chr13:52922200-52924400 | Enhancers | NHEK | skin |
7 | chr13:52922200-52924600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
8 | chr13:52923000-52924400 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
9 | chr13:52923200-52925000 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
10 | chr13:52923400-52929800 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
11 | chr13:52923600-52925600 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
12 | chr13:52923600-52927000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
13 | chr13:52923600-52927200 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
14 | chr13:52923600-52930200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
15 | chr13:52923800-52927000 | Weak transcription | NHLF | lung |
16 | chr13:52923800-52927200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
17 | chr13:52924000-52927000 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
18 | chr13:52924000-52927000 | Weak transcription | HSMMtube | muscle |
19 | chr13:52924000-52927000 | Weak transcription | NHDF-Ad | bronchial |
20 | chr13:52924000-52927200 | Weak transcription | HSMM | muscle |
21 | chr13:52924000-52930000 | Weak transcription | Hela-S3 | cervix |
22 | chr13:52924200-52927200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
23 | chr13:52924200-52927200 | Weak transcription | NH-A | brain |