Variant report
Variant | rs62318642 |
---|---|
Chromosome Location | chr4:98824949-98824950 |
allele | A/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] |
---|---|
rs10007663 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10007872 | 0.81[EUR][1000 genomes] |
rs10014284 | 0.91[ASN][1000 genomes] |
rs10017530 | 0.83[EUR][1000 genomes] |
rs10021044 | 0.81[EUR][1000 genomes] |
rs10025364 | 0.84[EUR][1000 genomes] |
rs10029372 | 0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10033994 | 0.84[EUR][1000 genomes] |
rs10034619 | 0.85[EUR][1000 genomes] |
rs11097582 | 0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11727653 | 0.81[EUR][1000 genomes] |
rs11735105 | 0.84[EUR][1000 genomes] |
rs11932942 | 0.81[EUR][1000 genomes] |
rs12163918 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13115356 | 0.83[EUR][1000 genomes] |
rs13118892 | 0.84[EUR][1000 genomes] |
rs13118945 | 0.84[EUR][1000 genomes] |
rs13121558 | 0.81[EUR][1000 genomes] |
rs13121766 | 0.84[EUR][1000 genomes] |
rs13122456 | 0.84[EUR][1000 genomes] |
rs13122897 | 0.84[EUR][1000 genomes] |
rs13124904 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13125930 | 0.86[ASN][1000 genomes] |
rs13127542 | 0.84[EUR][1000 genomes] |
rs13136930 | 0.83[EUR][1000 genomes] |
rs13137152 | 0.84[EUR][1000 genomes] |
rs13140514 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs13146909 | 0.84[EUR][1000 genomes] |
rs13147768 | 0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13148324 | 0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1426661 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1527516 | 0.84[EUR][1000 genomes] |
rs17026973 | 0.91[ASN][1000 genomes] |
rs17027058 | 0.88[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs17484890 | 0.81[EUR][1000 genomes] |
rs17484966 | 0.81[EUR][1000 genomes] |
rs17549003 | 0.84[EUR][1000 genomes] |
rs17550735 | 0.81[EUR][1000 genomes] |
rs1834647 | 0.88[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1834648 | 0.82[EUR][1000 genomes] |
rs1852545 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1869897 | 0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2114426 | 0.84[EUR][1000 genomes] |
rs2839836 | 0.84[EUR][1000 genomes] |
rs28415600 | 0.81[EUR][1000 genomes] |
rs28417716 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs28619044 | 0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs28622458 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs28761309 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs28791018 | 0.82[EUR][1000 genomes] |
rs34164616 | 0.81[EUR][1000 genomes] |
rs34313689 | 0.81[EUR][1000 genomes] |
rs34318449 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34528953 | 0.82[EUR][1000 genomes] |
rs34613258 | 0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs34892904 | 0.84[EUR][1000 genomes] |
rs35195511 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs35235971 | 0.81[EUR][1000 genomes] |
rs35491210 | 0.81[EUR][1000 genomes] |
rs35531558 | 0.84[EUR][1000 genomes] |
rs35644814 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs35685312 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs35752787 | 0.83[EUR][1000 genomes] |
rs35865860 | 0.84[EUR][1000 genomes] |
rs35951881 | 0.81[EUR][1000 genomes] |
rs36028444 | 0.84[EUR][1000 genomes] |
rs3852122 | 0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3852123 | 0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4502686 | 0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4699324 | 0.84[EUR][1000 genomes] |
rs4699595 | 0.81[EUR][1000 genomes] |
rs58367603 | 0.81[EUR][1000 genomes] |
rs59751489 | 0.84[EUR][1000 genomes] |
rs60007031 | 0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs60391193 | 0.84[EUR][1000 genomes] |
rs62318502 | 0.84[EUR][1000 genomes] |
rs62318503 | 0.84[EUR][1000 genomes] |
rs62318504 | 0.84[EUR][1000 genomes] |
rs62318644 | 0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs62321597 | 0.81[EUR][1000 genomes] |
rs62321598 | 0.81[EUR][1000 genomes] |
rs6817645 | 0.81[EUR][1000 genomes] |
rs6819047 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6827516 | 0.84[EUR][1000 genomes] |
rs6831925 | 0.84[EUR][1000 genomes] |
rs6839277 | 0.81[EUR][1000 genomes] |
rs6840669 | 0.81[EUR][1000 genomes] |
rs6843777 | 0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6848786 | 0.84[EUR][1000 genomes] |
rs6854919 | 0.84[EUR][1000 genomes] |
rs7657179 | 0.84[EUR][1000 genomes] |
rs7659006 | 0.84[EUR][1000 genomes] |
rs7659593 | 0.83[EUR][1000 genomes] |
rs7659801 | 0.83[EUR][1000 genomes] |
rs7663438 | 0.81[EUR][1000 genomes] |
rs7663661 | 0.81[EUR][1000 genomes] |
rs7664051 | 0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7672127 | 0.82[EUR][1000 genomes] |
rs7672720 | 0.82[EUR][1000 genomes] |
rs7672901 | 0.82[EUR][1000 genomes] |
rs7674407 | 0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7680909 | 0.84[EUR][1000 genomes] |
rs7682991 | 0.84[EUR][1000 genomes] |
rs7687958 | 0.81[EUR][1000 genomes] |
rs7691433 | 0.84[EUR][1000 genomes] |
rs7691864 | 0.85[EUR][1000 genomes] |
rs7696686 | 0.84[EUR][1000 genomes] |
rs7696715 | 0.82[EUR][1000 genomes] |
rs7697315 | 0.82[EUR][1000 genomes] |
rs880470 | 0.84[EUR][1000 genomes] |
rs921521 | 0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9992281 | 0.84[EUR][1000 genomes] |
rs9992360 | 0.84[EUR][1000 genomes] |
rs9992391 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9996098 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9998803 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv879643 | chr4:98317295-99065480 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv868914 | chr4:98416047-98969285 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1012612 | chr4:98433491-98949873 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | esv3502787 | chr4:98459061-98825579 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv3502788 | chr4:98459061-98825579 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1002098 | chr4:98501337-99086320 | Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
7 | nsv537193 | chr4:98501337-99086320 | ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
8 | nsv529623 | chr4:98501338-99460166 | Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
9 | nsv1010982 | chr4:98529206-98841438 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
10 | nsv537194 | chr4:98529206-98841438 | Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
11 | nsv879648 | chr4:98547717-99104879 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
12 | nsv1000011 | chr4:98562308-99101692 | Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
13 | nsv879649 | chr4:98652600-98873667 | Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
14 | nsv932060 | chr4:98696832-98902498 | ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
15 | nsv1000956 | chr4:98732458-99178588 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
16 | nsv999087 | chr4:98737003-98860303 | Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
17 | nsv594937 | chr4:98748299-98866902 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
18 | nsv530387 | chr4:98757752-98922248 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
19 | nsv1005567 | chr4:98779722-99031934 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
20 | nsv995045 | chr4:98802844-99022958 | ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:98821800-98832400 | Weak transcription | H1 Cell Line | embryonic stem cell |
2 | chr4:98824600-98825200 | Active TSS | ES-I3 Cell Line | embryonic stem cell |
3 | chr4:98824600-98825200 | Active TSS | ES-WA7 Cell Line | embryonic stem cell |
4 | chr4:98824600-98825200 | Active TSS | HUES48 Cell Line | embryonic stem cell |
5 | chr4:98824600-98825200 | Active TSS | HUES6 Cell Line | embryonic stem cell |
6 | chr4:98824800-98825000 | Flanking Active TSS | HUES64 Cell Line | embryonic stem cell |
7 | chr4:98824800-98825000 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
8 | chr4:98824800-98825200 | Active TSS | H9 Cell Line | embryonic stem cell |
9 | chr4:98824800-98825200 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
10 | chr4:98824800-98825200 | Active TSS | iPS-15b Cell Line | embryonic stem cell |
11 | chr4:98824800-98825200 | Active TSS | iPS-18 Cell Line | embryonic stem cell |