Variant report
Variant | rs34596457 |
---|---|
Chromosome Location | chr2:178704471-178704472 |
allele | G/T |
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 | chr2:178702452..178704995-chr2:178705681..178708457,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10168170 | 0.90[EUR][1000 genomes] |
rs10171247 | 0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs10186953 | 0.94[EUR][1000 genomes] |
rs10189134 | 0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs10197329 | 0.80[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs10200643 | 0.98[EUR][1000 genomes] |
rs10221806 | 0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs10497477 | 0.94[EUR][1000 genomes] |
rs10497478 | 0.94[EUR][1000 genomes] |
rs12693123 | 0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12693127 | 0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs12693151 | 0.94[EUR][1000 genomes] |
rs12993389 | 0.90[EUR][1000 genomes] |
rs13002398 | 0.94[EUR][1000 genomes] |
rs13010993 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs13017026 | 0.90[EUR][1000 genomes] |
rs13017462 | 0.94[EUR][1000 genomes] |
rs13017473 | 0.94[EUR][1000 genomes] |
rs13019623 | 0.94[EUR][1000 genomes] |
rs13021204 | 0.98[EUR][1000 genomes] |
rs13022267 | 0.90[EUR][1000 genomes] |
rs13023049 | 0.90[EUR][1000 genomes] |
rs13023495 | 0.86[EUR][1000 genomes] |
rs13023939 | 0.90[EUR][1000 genomes] |
rs13026481 | 0.90[EUR][1000 genomes] |
rs13027582 | 0.90[EUR][1000 genomes] |
rs13028692 | 0.90[EUR][1000 genomes] |
rs13034432 | 0.94[EUR][1000 genomes] |
rs13388218 | 0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs13389574 | 0.94[EUR][1000 genomes] |
rs13392577 | 0.98[EUR][1000 genomes] |
rs13393722 | 0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13395159 | 0.94[EUR][1000 genomes] |
rs13402629 | 0.94[EUR][1000 genomes] |
rs13402636 | 0.94[EUR][1000 genomes] |
rs13405585 | 0.90[EUR][1000 genomes] |
rs13406131 | 0.94[EUR][1000 genomes] |
rs13408518 | 0.90[EUR][1000 genomes] |
rs13408911 | 0.94[EUR][1000 genomes] |
rs13415041 | 0.94[EUR][1000 genomes] |
rs13419437 | 0.81[AFR][1000 genomes] |
rs13422706 | 0.98[EUR][1000 genomes] |
rs13423344 | 0.98[EUR][1000 genomes] |
rs13426862 | 0.98[EUR][1000 genomes] |
rs13429445 | 0.98[EUR][1000 genomes] |
rs1358299 | 0.82[AFR][1000 genomes] |
rs17330012 | 0.94[EUR][1000 genomes] |
rs17330172 | 0.94[EUR][1000 genomes] |
rs17330290 | 0.90[EUR][1000 genomes] |
rs17330381 | 0.90[EUR][1000 genomes] |
rs17401293 | 0.98[EUR][1000 genomes] |
rs17401951 | 0.94[EUR][1000 genomes] |
rs17402102 | 0.94[EUR][1000 genomes] |
rs17635803 | 0.90[EUR][1000 genomes] |
rs17635875 | 0.90[EUR][1000 genomes] |
rs17635934 | 0.86[EUR][1000 genomes] |
rs17635957 | 0.86[EUR][1000 genomes] |
rs17687170 | 0.86[EUR][1000 genomes] |
rs17687217 | 0.86[EUR][1000 genomes] |
rs2056715 | 0.86[EUR][1000 genomes] |
rs34018298 | 0.90[EUR][1000 genomes] |
rs34081471 | 0.90[EUR][1000 genomes] |
rs34206020 | 0.94[EUR][1000 genomes] |
rs34234621 | 0.90[EUR][1000 genomes] |
rs34363929 | 0.94[EUR][1000 genomes] |
rs34406776 | 0.90[EUR][1000 genomes] |
rs34434094 | 0.86[EUR][1000 genomes] |
rs34473720 | 0.94[EUR][1000 genomes] |
rs34479958 | 0.86[EUR][1000 genomes] |
rs34510795 | 0.90[EUR][1000 genomes] |
rs34528505 | 0.94[EUR][1000 genomes] |
rs34767203 | 0.98[EUR][1000 genomes] |
rs34948302 | 0.94[EUR][1000 genomes] |
rs35233809 | 0.94[EUR][1000 genomes] |
rs35286879 | 0.90[EUR][1000 genomes] |
rs35290022 | 0.86[EUR][1000 genomes] |
rs35454650 | 0.90[EUR][1000 genomes] |
rs35591668 | 0.86[EUR][1000 genomes] |
rs35699369 | 0.90[EUR][1000 genomes] |
rs35757742 | 0.86[EUR][1000 genomes] |
rs35797524 | 0.86[EUR][1000 genomes] |
rs35924394 | 0.94[EUR][1000 genomes] |
rs35952531 | 0.94[EUR][1000 genomes] |
rs6738614 | 0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs71423523 | 0.94[EUR][1000 genomes] |
rs71423534 | 0.84[EUR][1000 genomes] |
rs71423535 | 0.90[EUR][1000 genomes] |
rs71423537 | 0.90[EUR][1000 genomes] |
rs71423538 | 0.90[EUR][1000 genomes] |
rs71423539 | 0.90[EUR][1000 genomes] |
rs71423540 | 0.90[EUR][1000 genomes] |
rs71423541 | 0.90[EUR][1000 genomes] |
rs7575322 | 0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9989802 | 0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999086 | chr2:178262348-178773585 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
2 | nsv536055 | chr2:178262348-178773585 | Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
3 | nsv583690 | chr2:178638381-178712283 | Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv3053 | chr2:178690640-178735132 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:178696400-178705200 | Weak transcription | Psoas Muscle | Psoas |
2 | chr2:178699800-178716600 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
3 | chr2:178704000-178709000 | Weak transcription | Pancreas | Pancrea |