Variant report
Variant | rs3922681 |
---|---|
Chromosome Location | chr6:25698481-25698482 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
(count:1 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-HIST1H2BA-3 | chr6:25698265-25698930 | NONHSAT108167 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000146047 | Chromatin interaction |
ENSG00000164508 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10946793 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1141034 | 0.81[CEU][hapmap] |
rs1165156 | 0.81[CEU][hapmap] |
rs11794 | 1.00[CEU][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12190612 | 0.93[EUR][1000 genomes] |
rs12192077 | 0.93[EUR][1000 genomes] |
rs12194699 | 0.94[EUR][1000 genomes] |
rs12203927 | 0.93[EUR][1000 genomes] |
rs12209856 | 0.81[CEU][hapmap] |
rs12529272 | 0.94[EUR][1000 genomes] |
rs12662869 | 0.88[CEU][hapmap] |
rs12663099 | 0.87[CEU][hapmap];0.93[EUR][1000 genomes] |
rs1575535 | 0.81[CEU][hapmap] |
rs17267614 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17320090 | 0.96[EUR][1000 genomes] |
rs1892254 | 0.91[EUR][1000 genomes] |
rs1892255 | 0.91[EUR][1000 genomes] |
rs1937131 | 0.93[EUR][1000 genomes] |
rs1937132 | 0.91[EUR][1000 genomes] |
rs2000351 | 0.88[CEU][hapmap] |
rs2294346 | 0.80[ASN][1000 genomes] |
rs35969734 | 0.91[EUR][1000 genomes] |
rs3922699 | 0.87[CEU][hapmap];0.93[EUR][1000 genomes] |
rs3922842 | 0.87[CEU][hapmap];0.92[EUR][1000 genomes] |
rs3923725 | 0.85[CEU][hapmap];0.93[EUR][1000 genomes] |
rs4077878 | 0.96[EUR][1000 genomes] |
rs4131670 | 0.87[CEU][hapmap];0.93[EUR][1000 genomes] |
rs4132072 | 0.88[CEU][hapmap];0.96[EUR][1000 genomes] |
rs4145216 | 0.93[EUR][1000 genomes] |
rs4145217 | 0.93[EUR][1000 genomes] |
rs4145218 | 0.93[EUR][1000 genomes] |
rs4360128 | 0.86[CEU][hapmap];0.92[EUR][1000 genomes] |
rs4464787 | 0.82[CEU][hapmap];0.93[EUR][1000 genomes] |
rs4612154 | 0.87[ASN][1000 genomes] |
rs4711093 | 0.88[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4711094 | 0.92[EUR][1000 genomes] |
rs4711095 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs4711096 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs4711097 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs4711098 | 0.93[EUR][1000 genomes] |
rs4711099 | 0.93[EUR][1000 genomes] |
rs4711100 | 0.93[EUR][1000 genomes] |
rs4711101 | 0.92[EUR][1000 genomes] |
rs4711102 | 0.93[EUR][1000 genomes] |
rs4711103 | 0.93[EUR][1000 genomes] |
rs4711104 | 0.83[EUR][1000 genomes] |
rs4712956 | 0.94[EUR][1000 genomes] |
rs4712957 | 0.94[EUR][1000 genomes] |
rs4712959 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs4712960 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs4712961 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs4712963 | 0.93[EUR][1000 genomes] |
rs4712964 | 0.93[EUR][1000 genomes] |
rs4712965 | 0.93[EUR][1000 genomes] |
rs4712967 | 0.93[EUR][1000 genomes] |
rs61297482 | 0.96[EUR][1000 genomes] |
rs6456694 | 1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.98[EUR][1000 genomes] |
rs6456696 | 0.93[EUR][1000 genomes] |
rs6456697 | 0.93[EUR][1000 genomes] |
rs6456699 | 0.92[EUR][1000 genomes] |
rs6908407 | 0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6908713 | 0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6923839 | 0.89[EUR][1000 genomes] |
rs6924782 | 0.93[EUR][1000 genomes] |
rs6924794 | 0.88[CEU][hapmap];0.93[EUR][1000 genomes] |
rs6941933 | 0.93[EUR][1000 genomes] |
rs7450798 | 0.88[CEU][hapmap];0.96[EUR][1000 genomes] |
rs7453371 | 0.96[EUR][1000 genomes] |
rs760698 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7746502 | 0.83[EUR][1000 genomes] |
rs7746609 | 0.84[EUR][1000 genomes] |
rs7749149 | 0.88[CEU][hapmap] |
rs7754296 | 0.93[EUR][1000 genomes] |
rs7754733 | 0.93[EUR][1000 genomes] |
rs7754814 | 0.93[EUR][1000 genomes] |
rs7765833 | 0.87[EUR][1000 genomes] |
rs7770037 | 0.88[CEU][hapmap] |
rs7772382 | 0.98[EUR][1000 genomes] |
rs7775354 | 0.93[EUR][1000 genomes] |
rs9348692 | 0.87[CEU][hapmap];0.90[AFR][1000 genomes];0.98[EUR][1000 genomes] |
rs9348694 | 1.00[CEU][hapmap];0.91[EUR][1000 genomes] |
rs9356984 | 1.00[CEU][hapmap];0.96[EUR][1000 genomes] |
rs9356985 | 0.93[EUR][1000 genomes] |
rs9356986 | 0.86[CEU][hapmap];0.93[EUR][1000 genomes] |
rs9356987 | 0.87[CEU][hapmap];0.93[EUR][1000 genomes] |
rs9356988 | 0.82[CEU][hapmap] |
rs9358871 | 0.87[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9358872 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9358873 | 0.86[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9358875 | 0.86[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9358876 | 0.87[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9358877 | 0.87[CEU][hapmap];0.93[EUR][1000 genomes] |
rs9358878 | 0.93[EUR][1000 genomes] |
rs9358879 | 0.92[EUR][1000 genomes] |
rs9358880 | 0.93[EUR][1000 genomes] |
rs9358881 | 0.93[EUR][1000 genomes] |
rs9358883 | 0.91[EUR][1000 genomes] |
rs9358884 | 0.91[EUR][1000 genomes] |
rs9358885 | 0.91[EUR][1000 genomes] |
rs9358886 | 0.88[CEU][hapmap];0.89[EUR][1000 genomes] |
rs9366627 | 1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9366628 | 0.94[EUR][1000 genomes] |
rs9366629 | 0.93[EUR][1000 genomes] |
rs9379778 | 0.88[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9379779 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9379781 | 0.94[EUR][1000 genomes] |
rs9379782 | 0.92[AFR][1000 genomes];0.98[EUR][1000 genomes] |
rs9379783 | 1.00[CEU][hapmap];0.96[EUR][1000 genomes] |
rs9379784 | 0.88[CEU][hapmap];0.97[EUR][1000 genomes] |
rs9379785 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9379786 | 0.87[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9379788 | 0.93[EUR][1000 genomes] |
rs9379789 | 0.93[EUR][1000 genomes] |
rs9379791 | 0.91[EUR][1000 genomes] |
rs9393655 | 0.96[EUR][1000 genomes] |
rs9393656 | 0.95[EUR][1000 genomes] |
rs9393658 | 0.94[EUR][1000 genomes] |
rs9393659 | 0.93[EUR][1000 genomes] |
rs9393661 | 0.87[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9393662 | 0.88[CEU][hapmap];0.93[EUR][1000 genomes] |
rs9393663 | 0.93[EUR][1000 genomes] |
rs9393665 | 0.93[EUR][1000 genomes] |
rs9467571 | 0.82[ASN][1000 genomes] |
rs9467572 | 0.97[EUR][1000 genomes];0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv883488 | chr6:25592489-25731691 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1029920 | chr6:25638507-26585842 | Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1215 gene(s) | inside rSNPs | diseases |
3 | nsv538162 | chr6:25638507-26585842 | Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1215 gene(s) | inside rSNPs | diseases |
4 | nsv427747 | chr6:25641380-25908218 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:25695400-25700000 | Enhancers | K562 | blood |
2 | chr6:25697800-25698600 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
3 | chr6:25698000-25699000 | Enhancers | Hela-S3 | cervix |