Variant report
Variant | rs1039288 |
---|---|
Chromosome Location | chr1:197821607-197821608 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
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rs_ID | r2[population] |
---|---|
rs1039287 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10922308 | 0.87[EUR][1000 genomes] |
rs10922309 | 0.89[EUR][1000 genomes] |
rs10922310 | 0.89[EUR][1000 genomes] |
rs10922311 | 0.89[EUR][1000 genomes] |
rs10922312 | 0.87[EUR][1000 genomes] |
rs10922314 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs11800139 | 1.00[EUR][1000 genomes] |
rs12062450 | 0.87[EUR][1000 genomes] |
rs12079329 | 0.88[EUR][1000 genomes] |
rs12079525 | 0.87[EUR][1000 genomes] |
rs1499601 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs16842055 | 0.89[EUR][1000 genomes] |
rs17567921 | 1.00[CEU][hapmap] |
rs17641842 | 1.00[CEU][hapmap] |
rs2047540 | 0.84[EUR][1000 genomes] |
rs2047541 | 0.87[EUR][1000 genomes] |
rs2358488 | 0.88[EUR][1000 genomes] |
rs6661330 | 1.00[CEU][hapmap] |
rs6685897 | 0.81[EUR][1000 genomes] |
rs74137403 | 0.85[EUR][1000 genomes] |
rs74137406 | 0.82[EUR][1000 genomes] |
rs74137408 | 0.82[EUR][1000 genomes] |
rs7415533 | 0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1009697 | chr1:197804294-197825037 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:197821600-197822800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |