Variant report
Variant | rs10243984 |
---|---|
Chromosome Location | chr7:145992945-145992946 |
allele | C/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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:145988038..145989736-chr7:145992431..145994390,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10255068 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10255186 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10276235 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10277301 | 0.89[ASN][1000 genomes] |
rs10282451 | 0.89[ASN][1000 genomes] |
rs2693299 | 0.96[ASN][1000 genomes] |
rs28379982 | 0.84[ASN][1000 genomes] |
rs28512358 | 0.84[ASN][1000 genomes] |
rs58749345 | 0.88[ASN][1000 genomes] |
rs59186277 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6958305 | 0.84[ASN][1000 genomes] |
rs6973230 | 0.88[ASN][1000 genomes] |
rs6973797 | 0.88[ASN][1000 genomes] |
rs73162171 | 0.92[ASN][1000 genomes] |
rs73162193 | 0.84[ASN][1000 genomes] |
rs73162194 | 0.84[ASN][1000 genomes] |
rs73162195 | 0.88[ASN][1000 genomes] |
rs73162196 | 0.88[ASN][1000 genomes] |
rs7790714 | 0.92[ASN][1000 genomes] |
rs7794124 | 0.92[ASN][1000 genomes] |
rs7795585 | 1.00[ASN][1000 genomes] |
rs7807111 | 0.89[ASN][1000 genomes] |
rs802506 | 1.00[ASN][1000 genomes] |
rs802508 | 0.96[ASN][1000 genomes] |
rs802510 | 0.96[ASN][1000 genomes] |
rs802511 | 1.00[ASN][1000 genomes] |
rs802512 | 1.00[ASN][1000 genomes] |
rs802513 | 1.00[ASN][1000 genomes] |
rs802514 | 0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs802526 | 1.00[ASN][1000 genomes] |
rs802527 | 1.00[ASN][1000 genomes] |
rs802558 | 0.96[ASN][1000 genomes] |
rs802559 | 0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv889384 | chr7:145541783-146239545 | Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1020950 | chr7:145683419-146264304 | Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1030541 | chr7:145883107-146022564 | Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv889387 | chr7:145903862-146239545 | Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv533345 | chr7:145934546-146134958 | Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv933622 | chr7:145935381-145995971 | Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv5993 | chr7:145970629-146015976 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:145992800-145993600 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |