Variant report
Variant | rs9327866 |
---|---|
Chromosome Location | chr5:101919043-101919044 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:101918491..101920425-chr5:102376552..102378395,7 | MCF-7 | breast: | |
2 | chr5:101919006..101919896-chr5:102005661..102006572,4 | MCF-7 | breast: | |
3 | chr5:101917966..101921211-chr5:101923509..101926669,3 | K562 | blood: | |
4 | chr5:101918211..101920924-chr5:102375515..102377060,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10035507 | 1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs10038730 | 1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs10041969 | 1.00[JPT][hapmap] |
rs10045929 | 1.00[JPT][hapmap] |
rs10051006 | 1.00[JPT][hapmap] |
rs10057940 | 1.00[ASN][1000 genomes] |
rs10059568 | 1.00[ASN][1000 genomes] |
rs10059604 | 1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10060403 | 1.00[JPT][hapmap] |
rs10066065 | 1.00[ASN][1000 genomes] |
rs10069964 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10070269 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10073454 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10075530 | 1.00[JPT][hapmap] |
rs10077046 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10477819 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10479213 | 1.00[JPT][hapmap] |
rs10479237 | 0.97[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10515328 | 0.93[ASN][1000 genomes] |
rs10515329 | 0.93[ASN][1000 genomes] |
rs13357560 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13358233 | 1.00[JPT][hapmap] |
rs13361792 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1452063 | 1.00[JPT][hapmap] |
rs1502843 | 0.93[ASN][1000 genomes] |
rs1502850 | 0.93[ASN][1000 genomes] |
rs17150488 | 1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs17151033 | 1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs17151574 | 0.93[ASN][1000 genomes] |
rs17152198 | 1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs28415625 | 0.93[ASN][1000 genomes] |
rs41389647 | 1.00[JPT][hapmap] |
rs56181501 | 0.93[ASN][1000 genomes] |
rs58139210 | 0.93[ASN][1000 genomes] |
rs6596500 | 0.93[ASN][1000 genomes] |
rs6862833 | 0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6866284 | 0.91[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6870113 | 0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6870270 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6876722 | 1.00[JPT][hapmap] |
rs6883528 | 1.00[JPT][hapmap] |
rs6885350 | 1.00[JPT][hapmap] |
rs6885781 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6885940 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6890447 | 0.89[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6898458 | 1.00[JPT][hapmap];0.93[ASN][1000 genomes] |
rs72779996 | 0.93[ASN][1000 genomes] |
rs72779997 | 0.93[ASN][1000 genomes] |
rs7705924 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7709217 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7728204 | 0.93[ASN][1000 genomes] |
rs9686862 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9687561 | 0.97[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817537 | chr5:101489151-101992104 | Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv1016176 | chr5:101534391-102333606 | Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
3 | nsv537831 | chr5:101534391-102333606 | Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
4 | nsv1029894 | chr5:101620079-102516827 | Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
5 | nsv830428 | chr5:101797242-101958791 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
6 | nsv1033193 | chr5:101859229-102420837 | Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
7 | nsv1033405 | chr5:101912749-102005038 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:101917800-101919800 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
2 | chr5:101918200-101919800 | Enhancers | NHDF-Ad | bronchial |
3 | chr5:101918400-101919800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr5:101918600-101919200 | Enhancers | HSMM | muscle |
5 | chr5:101918600-101919800 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
6 | chr5:101919000-101920000 | Enhancers | Fetal Brain Female | brain |
7 | chr5:101919000-101920800 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |