Variant report
Variant | rs2899448 |
---|---|
Chromosome Location | chr15:49978375-49978376 |
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 | chr15:49977822..49979343-chr15:50042316..50044829,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10152754 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10152787 | 0.82[EUR][1000 genomes] |
rs10162802 | 0.81[EUR][1000 genomes] |
rs10467920 | 0.81[EUR][1000 genomes] |
rs1048348 | 0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11070708 | 0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11070713 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11631904 | 0.81[EUR][1000 genomes] |
rs11632201 | 0.81[ASN][1000 genomes] |
rs11632674 | 0.81[EUR][1000 genomes] |
rs11634751 | 0.81[EUR][1000 genomes] |
rs11636378 | 0.81[EUR][1000 genomes] |
rs11857320 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12185128 | 0.81[EUR][1000 genomes] |
rs12437899 | 0.81[EUR][1000 genomes] |
rs12440099 | 0.81[EUR][1000 genomes] |
rs12441304 | 0.81[EUR][1000 genomes] |
rs12905627 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1395902 | 0.81[EUR][1000 genomes] |
rs1507618 | 0.84[AFR][1000 genomes] |
rs1588131 | 0.81[EUR][1000 genomes] |
rs1588132 | 0.81[EUR][1000 genomes] |
rs1605477 | 0.81[EUR][1000 genomes] |
rs1605478 | 0.81[EUR][1000 genomes] |
rs1605479 | 0.81[EUR][1000 genomes] |
rs1605484 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs17482113 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1848289 | 0.81[EUR][1000 genomes] |
rs1857992 | 0.83[EUR][1000 genomes] |
rs1874612 | 0.81[EUR][1000 genomes] |
rs1911614 | 0.81[EUR][1000 genomes] |
rs2413953 | 0.81[EUR][1000 genomes] |
rs2601020 | 0.88[EUR][1000 genomes] |
rs28562087 | 0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs28788326 | 0.81[EUR][1000 genomes] |
rs28822970 | 0.81[EUR][1000 genomes] |
rs28842346 | 0.81[EUR][1000 genomes] |
rs28871940 | 0.81[EUR][1000 genomes] |
rs4303431 | 0.81[EUR][1000 genomes] |
rs4775817 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs55993510 | 0.83[EUR][1000 genomes] |
rs56094557 | 0.81[EUR][1000 genomes] |
rs56335122 | 0.81[EUR][1000 genomes] |
rs56692783 | 0.81[EUR][1000 genomes] |
rs57421305 | 0.83[EUR][1000 genomes] |
rs57980364 | 0.81[EUR][1000 genomes] |
rs57997677 | 0.81[EUR][1000 genomes] |
rs60728602 | 0.81[EUR][1000 genomes] |
rs62009983 | 0.81[EUR][1000 genomes] |
rs62021583 | 0.81[EUR][1000 genomes] |
rs62021584 | 0.81[EUR][1000 genomes] |
rs62021585 | 0.81[EUR][1000 genomes] |
rs62021586 | 0.81[EUR][1000 genomes] |
rs62021587 | 0.81[EUR][1000 genomes] |
rs6493376 | 0.81[EUR][1000 genomes] |
rs67428220 | 0.81[EUR][1000 genomes] |
rs67916122 | 0.81[EUR][1000 genomes] |
rs68095295 | 0.82[EUR][1000 genomes] |
rs692008 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7162351 | 0.81[EUR][1000 genomes] |
rs7162792 | 0.81[EUR][1000 genomes] |
rs7163740 | 0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7164283 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7166202 | 0.81[EUR][1000 genomes] |
rs7167429 | 0.81[EUR][1000 genomes] |
rs7168031 | 0.81[EUR][1000 genomes] |
rs7176306 | 0.81[AFR][1000 genomes] |
rs7176350 | 0.81[EUR][1000 genomes] |
rs7177247 | 0.82[EUR][1000 genomes] |
rs7178194 | 0.81[EUR][1000 genomes] |
rs7181916 | 0.81[EUR][1000 genomes] |
rs7182072 | 0.81[EUR][1000 genomes] |
rs7183313 | 0.81[EUR][1000 genomes] |
rs731051 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs733097 | 0.81[EUR][1000 genomes] |
rs8029561 | 0.81[EUR][1000 genomes] |
rs8030761 | 0.81[EUR][1000 genomes] |
rs8033476 | 0.94[AFR][1000 genomes] |
rs8034202 | 0.81[EUR][1000 genomes] |
rs8035468 | 0.83[EUR][1000 genomes] |
rs8036139 | 0.81[EUR][1000 genomes] |
rs8041493 | 0.81[EUR][1000 genomes] |
rs925103 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs962710 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9635335 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv431388 | chr15:49835663-49997483 | Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
2 | nsv1044277 | chr15:49921547-50702386 | Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 107 gene(s) | inside rSNPs | diseases |
3 | nsv542380 | chr15:49921547-50702386 | Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 107 gene(s) | inside rSNPs | diseases |
4 | nsv569393 | chr15:49977687-50012256 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:49966800-49987400 | Weak transcription | NHLF | lung |