Variant report
Variant | rs61957307 |
---|---|
Chromosome Location | chr13:52803479-52803480 |
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 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs35975899 | 1.00[ASN][1000 genomes] |
rs41292810 | 1.00[ASN][1000 genomes] |
rs41292818 | 1.00[ASN][1000 genomes] |
rs55715265 | 0.90[EUR][1000 genomes] |
rs55850688 | 1.00[ASN][1000 genomes] |
rs56173235 | 1.00[ASN][1000 genomes] |
rs56249382 | 0.91[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs57412438 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs57831032 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs57904860 | 1.00[ASN][1000 genomes] |
rs58655347 | 1.00[ASN][1000 genomes] |
rs60322427 | 1.00[ASN][1000 genomes] |
rs60406129 | 1.00[ASN][1000 genomes] |
rs61011708 | 1.00[ASN][1000 genomes] |
rs61171418 | 1.00[ASN][1000 genomes] |
rs61677410 | 1.00[ASN][1000 genomes] |
rs61957231 | 0.84[EUR][1000 genomes] |
rs61957232 | 0.84[EUR][1000 genomes] |
rs61957238 | 0.87[EUR][1000 genomes] |
rs61957248 | 0.87[EUR][1000 genomes] |
rs61957252 | 0.87[EUR][1000 genomes] |
rs61957253 | 0.87[EUR][1000 genomes] |
rs61957254 | 0.87[EUR][1000 genomes] |
rs61957255 | 0.84[EUR][1000 genomes] |
rs61957256 | 0.87[EUR][1000 genomes] |
rs61957966 | 0.87[ASN][1000 genomes] |
rs61957967 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs61957976 | 1.00[ASN][1000 genomes] |
rs61957977 | 1.00[ASN][1000 genomes] |
rs61957978 | 1.00[ASN][1000 genomes] |
rs61957980 | 1.00[ASN][1000 genomes] |
rs61957981 | 1.00[ASN][1000 genomes] |
rs61957982 | 1.00[ASN][1000 genomes] |
rs61957983 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs61957984 | 1.00[ASN][1000 genomes] |
rs61957986 | 1.00[ASN][1000 genomes] |
rs61957987 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs61957988 | 0.82[AMR][1000 genomes];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 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs61958010 | 1.00[ASN][1000 genomes] |
rs61958011 | 1.00[ASN][1000 genomes] |
rs61958012 | 0.82[AMR][1000 genomes];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 | 0.82[AMR][1000 genomes];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] |
rs61958806 | 0.87[EUR][1000 genomes] |
rs61958807 | 0.87[EUR][1000 genomes] |
rs61958860 | 0.87[EUR][1000 genomes] |
rs61958863 | 0.87[EUR][1000 genomes] |
rs61958865 | 0.87[EUR][1000 genomes] |
rs61959660 | 1.00[ASN][1000 genomes] |
rs61959661 | 1.00[ASN][1000 genomes] |
rs61959663 | 1.00[ASN][1000 genomes] |
rs61959664 | 0.81[AMR][1000 genomes];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] |
rs719349 | 0.87[EUR][1000 genomes] |
rs7331858 | 0.87[ASN][1000 genomes] |
rs7333070 | 0.90[EUR][1000 genomes] |
rs7983047 | 1.00[ASN][1000 genomes] |
rs9526881 | 0.86[ASN][1000 genomes] |
rs9526882 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9526888 | 1.00[ASN][1000 genomes] |
rs9526890 | 1.00[ASN][1000 genomes] |
rs9526892 | 1.00[ASN][1000 genomes] |
rs9526895 | 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 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9526910 | 1.00[ASN][1000 genomes] |
rs9526915 | 1.00[ASN][1000 genomes] |
rs9526916 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9526924 | 1.00[ASN][1000 genomes] |
rs9526926 | 1.00[ASN][1000 genomes] |
rs9535838 | 0.81[EUR][1000 genomes] |
rs9535839 | 0.87[EUR][1000 genomes] |
rs9535850 | 0.87[EUR][1000 genomes] |
rs9535859 | 0.81[EUR][1000 genomes] |
rs9535869 | 0.84[EUR][1000 genomes] |
rs9535870 | 0.84[EUR][1000 genomes] |
rs9535875 | 0.84[EUR][1000 genomes] |
rs9535886 | 0.83[EUR][1000 genomes] |
rs9535892 | 0.87[EUR][1000 genomes] |
rs9535897 | 0.87[EUR][1000 genomes] |
rs9535900 | 0.87[EUR][1000 genomes] |
rs9535901 | 0.87[EUR][1000 genomes] |
rs9535902 | 0.87[EUR][1000 genomes] |
rs9535910 | 0.87[EUR][1000 genomes] |
rs9535911 | 0.87[EUR][1000 genomes] |
rs9535913 | 0.87[EUR][1000 genomes] |
rs9535975 | 1.00[ASN][1000 genomes] |
rs9535991 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9536003 | 0.87[ASN][1000 genomes] |
rs9536004 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536005 | 1.00[ASN][1000 genomes] |
rs9536007 | 0.86[ASN][1000 genomes] |
rs9536008 | 1.00[ASN][1000 genomes] |
rs9536009 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536018 | 1.00[ASN][1000 genomes] |
rs9536019 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536020 | 1.00[ASN][1000 genomes] |
rs9536022 | 1.00[ASN][1000 genomes] |
rs9536023 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536025 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536026 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536027 | 1.00[ASN][1000 genomes] |
rs9536028 | 1.00[ASN][1000 genomes] |
rs9536029 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536031 | 1.00[ASN][1000 genomes] |
rs9536033 | 1.00[ASN][1000 genomes] |
rs9536034 | 0.82[AMR][1000 genomes];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 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536049 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536050 | 1.00[ASN][1000 genomes] |
rs9536051 | 1.00[ASN][1000 genomes] |
rs9536053 | 0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9536054 | 1.00[ASN][1000 genomes] |
rs9536056 | 0.82[AMR][1000 genomes];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 | 0.82[AMR][1000 genomes];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] |
rs9536098 | 0.84[AMR][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 | nsv530718 | chr13:52291802-52832752 | Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | nsv819887 | chr13:52772113-52926921 | Enhancers Active TSS Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
7 | nsv983588 | chr13:52772461-52833538 | Enhancers Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | n/a |
8 | nsv900083 | chr13:52783120-52885838 | Weak transcription Active TSS Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:52803200-52803600 | Enhancers | HUVEC | blood vessel |