Variant report
Variant | rs62154934 |
---|---|
Chromosome Location | chr2:98820521-98820522 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:98817636..98820635-chr2:98821090..98823040,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000231635 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17426979 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17427034 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17427096 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17427272 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17427314 | 1.00[AFR][1000 genomes] |
rs17427356 | 1.00[AFR][1000 genomes] |
rs17427531 | 1.00[AFR][1000 genomes] |
rs17427573 | 1.00[AFR][1000 genomes] |
rs17427636 | 1.00[AFR][1000 genomes] |
rs17427726 | 1.00[AFR][1000 genomes] |
rs17428000 | 1.00[AFR][1000 genomes] |
rs17428212 | 1.00[AFR][1000 genomes] |
rs17428262 | 1.00[AFR][1000 genomes] |
rs17428318 | 1.00[AFR][1000 genomes] |
rs17428528 | 1.00[AFR][1000 genomes] |
rs17428626 | 1.00[AFR][1000 genomes] |
rs17428843 | 1.00[AFR][1000 genomes] |
rs17429145 | 1.00[AFR][1000 genomes] |
rs17429278 | 1.00[AFR][1000 genomes] |
rs17492872 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17493076 | 1.00[AFR][1000 genomes] |
rs17493153 | 1.00[AFR][1000 genomes] |
rs17493543 | 1.00[AFR][1000 genomes] |
rs17493879 | 1.00[AFR][1000 genomes] |
rs17500449 | 1.00[AFR][1000 genomes] |
rs17500559 | 1.00[AFR][1000 genomes] |
rs17500893 | 1.00[AFR][1000 genomes] |
rs17501122 | 1.00[AFR][1000 genomes] |
rs4132465 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4132466 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154930 | 0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs62154931 | 0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs62154932 | 0.93[AMR][1000 genomes] |
rs62154933 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62154936 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62154937 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154939 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154940 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154941 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154942 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154943 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154944 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62154945 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62155276 | 1.00[AFR][1000 genomes] |
rs62155278 | 1.00[AFR][1000 genomes] |
rs62155279 | 1.00[AFR][1000 genomes] |
rs62155280 | 1.00[AFR][1000 genomes] |
rs62155282 | 1.00[AFR][1000 genomes] |
rs62155283 | 1.00[AFR][1000 genomes] |
rs62155284 | 1.00[AFR][1000 genomes] |
rs62155285 | 1.00[AFR][1000 genomes] |
rs62155286 | 1.00[AFR][1000 genomes] |
rs62155288 | 1.00[AFR][1000 genomes] |
rs62155289 | 1.00[AFR][1000 genomes] |
rs62155290 | 1.00[AFR][1000 genomes] |
rs62155291 | 1.00[AFR][1000 genomes] |
rs62155292 | 1.00[AFR][1000 genomes] |
rs62155293 | 1.00[AFR][1000 genomes] |
rs62155294 | 1.00[AFR][1000 genomes] |
rs62155295 | 1.00[AFR][1000 genomes] |
rs62155296 | 1.00[AFR][1000 genomes] |
rs62155297 | 1.00[AFR][1000 genomes] |
rs62155300 | 1.00[AFR][1000 genomes] |
rs62155301 | 1.00[AFR][1000 genomes] |
rs62155302 | 1.00[AFR][1000 genomes] |
rs62155303 | 1.00[AFR][1000 genomes] |
rs62155305 | 1.00[AFR][1000 genomes] |
rs62155308 | 1.00[AFR][1000 genomes] |
rs62155309 | 1.00[AFR][1000 genomes] |
rs62155310 | 1.00[AFR][1000 genomes] |
rs62155311 | 1.00[AFR][1000 genomes] |
rs62155314 | 1.00[AFR][1000 genomes] |
rs62155315 | 1.00[AFR][1000 genomes] |
rs62155316 | 1.00[AFR][1000 genomes] |
rs62155318 | 1.00[AFR][1000 genomes] |
rs62155348 | 1.00[AFR][1000 genomes] |
rs62155349 | 1.00[AFR][1000 genomes] |
rs62155351 | 1.00[AFR][1000 genomes] |
rs62155352 | 1.00[AFR][1000 genomes] |
rs62155353 | 1.00[AFR][1000 genomes] |
rs62155356 | 1.00[AFR][1000 genomes] |
rs62155357 | 1.00[AFR][1000 genomes] |
rs62155359 | 1.00[AFR][1000 genomes] |
rs62156260 | 1.00[AFR][1000 genomes] |
rs62156262 | 1.00[AFR][1000 genomes] |
rs62156275 | 1.00[AFR][1000 genomes] |
rs62156664 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156665 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156667 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156668 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156669 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156671 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156673 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156674 | 1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62156675 | 1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62156684 | 0.84[EUR][1000 genomes] |
rs62156685 | 0.84[EUR][1000 genomes] |
rs62156709 | 1.00[AFR][1000 genomes] |
rs62156710 | 1.00[AFR][1000 genomes] |
rs62156711 | 1.00[AFR][1000 genomes] |
rs62156722 | 1.00[AFR][1000 genomes] |
rs62156725 | 1.00[AFR][1000 genomes] |
rs62156726 | 1.00[AFR][1000 genomes] |
rs62156727 | 1.00[AFR][1000 genomes] |
rs62156728 | 1.00[AFR][1000 genomes] |
rs62156729 | 1.00[AFR][1000 genomes] |
rs62156730 | 1.00[AFR][1000 genomes] |
rs62156731 | 1.00[AFR][1000 genomes] |
rs62156732 | 1.00[AFR][1000 genomes] |
rs62156733 | 1.00[AFR][1000 genomes] |
rs62156738 | 1.00[AFR][1000 genomes] |
rs62156739 | 1.00[AFR][1000 genomes] |
rs62156741 | 1.00[AFR][1000 genomes] |
rs62156742 | 1.00[AFR][1000 genomes] |
rs62156743 | 1.00[AFR][1000 genomes] |
rs62157893 | 1.00[AFR][1000 genomes] |
rs62157895 | 1.00[AFR][1000 genomes] |
rs62157896 | 1.00[AFR][1000 genomes] |
rs62157897 | 1.00[AFR][1000 genomes] |
rs62157898 | 1.00[AFR][1000 genomes] |
rs62157899 | 1.00[AFR][1000 genomes] |
rs62157900 | 1.00[AFR][1000 genomes] |
rs62157902 | 1.00[AFR][1000 genomes] |
rs62157903 | 1.00[AFR][1000 genomes] |
rs62157904 | 1.00[AFR][1000 genomes] |
rs62157905 | 1.00[AFR][1000 genomes] |
rs62157906 | 1.00[AFR][1000 genomes] |
rs62157909 | 1.00[AFR][1000 genomes] |
rs62157910 | 1.00[AFR][1000 genomes] |
rs62157912 | 1.00[AFR][1000 genomes] |
rs62157913 | 1.00[AFR][1000 genomes] |
rs62157917 | 1.00[AFR][1000 genomes] |
rs62157918 | 1.00[AFR][1000 genomes] |
rs62157919 | 1.00[AFR][1000 genomes] |
rs62157920 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv521568 | chr2:98403683-98826203 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1003925 | chr2:98442640-98821102 | Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
3 | nsv518056 | chr2:98586842-99156296 | Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
4 | nsv1004082 | chr2:98792256-98967681 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
5 | nsv535833 | chr2:98792256-98967681 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |