Variant report
Variant | rs28556954 |
---|---|
Chromosome Location | chr8:49662318-49662319 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:49657699..49660104-chr8:49660800..49663399,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10089076 | 1.00[AMR][1000 genomes] |
rs10090292 | 1.00[AMR][1000 genomes] |
rs10094086 | 0.87[AFR][1000 genomes] |
rs10098793 | 1.00[AMR][1000 genomes] |
rs10099006 | 0.87[AFR][1000 genomes] |
rs10099443 | 1.00[AMR][1000 genomes] |
rs10100402 | 0.84[AFR][1000 genomes] |
rs10100701 | 1.00[AMR][1000 genomes] |
rs10104194 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10108968 | 0.84[AFR][1000 genomes] |
rs10109238 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10504068 | 0.90[AFR][1000 genomes] |
rs1384218 | 1.00[AMR][1000 genomes] |
rs16938326 | 1.00[AMR][1000 genomes] |
rs16938489 | 1.00[AMR][1000 genomes] |
rs16938498 | 1.00[AMR][1000 genomes] |
rs16938500 | 1.00[AMR][1000 genomes] |
rs16938602 | 1.00[AMR][1000 genomes] |
rs16938740 | 0.90[AFR][1000 genomes] |
rs16938748 | 0.90[AFR][1000 genomes] |
rs16938750 | 0.90[AFR][1000 genomes] |
rs16938756 | 0.90[AFR][1000 genomes] |
rs16938764 | 0.84[AFR][1000 genomes] |
rs16938765 | 0.84[AFR][1000 genomes] |
rs16938767 | 0.84[AFR][1000 genomes] |
rs28377247 | 0.84[AFR][1000 genomes] |
rs28477899 | 0.84[AFR][1000 genomes] |
rs28573934 | 1.00[AMR][1000 genomes] |
rs28702592 | 0.84[AFR][1000 genomes] |
rs28709071 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28772946 | 0.84[AFR][1000 genomes] |
rs28781607 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28817008 | 1.00[AMR][1000 genomes] |
rs28861728 | 0.87[AFR][1000 genomes] |
rs56177835 | 1.00[AMR][1000 genomes] |
rs56184941 | 0.84[AFR][1000 genomes] |
rs56787106 | 1.00[AMR][1000 genomes] |
rs56795854 | 1.00[AMR][1000 genomes] |
rs58750692 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60181153 | 0.84[AFR][1000 genomes] |
rs61184099 | 0.84[AFR][1000 genomes] |
rs61598535 | 1.00[AMR][1000 genomes] |
rs6472052 | 0.84[AFR][1000 genomes] |
rs6472053 | 0.84[AFR][1000 genomes] |
rs6988916 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7017560 | 1.00[AMR][1000 genomes] |
rs73678173 | 1.00[AMR][1000 genomes] |
rs73678187 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73678188 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73678200 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73678201 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73680707 | 0.90[AFR][1000 genomes] |
rs73680710 | 0.90[AFR][1000 genomes] |
rs73680711 | 0.90[AFR][1000 genomes] |
rs73680714 | 0.84[AFR][1000 genomes] |
rs73680715 | 0.84[AFR][1000 genomes] |
rs73680718 | 0.84[AFR][1000 genomes] |
rs7819693 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7823444 | 1.00[AMR][1000 genomes] |
rs7825162 | 0.90[AFR][1000 genomes] |
rs7826258 | 0.84[AFR][1000 genomes] |
rs7826724 | 0.90[AFR][1000 genomes] |
rs7838334 | 0.90[AFR][1000 genomes] |
rs7839672 | 0.84[AFR][1000 genomes] |
rs7842381 | 0.84[AFR][1000 genomes] |
rs9298065 | 0.90[AFR][1000 genomes] |
rs9657076 | 1.00[AMR][1000 genomes] |
rs9694357 | 1.00[AMR][1000 genomes] |
rs9886548 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2761425 | chr8:49658066-49669601 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:49656800-49662400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr8:49660400-49662400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr8:49661000-49668200 | Weak transcription | Pancreas | Pancrea |
4 | chr8:49661200-49662400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr8:49661400-49666000 | Weak transcription | Muscle Satellite Cultured Cells | -- |
6 | chr8:49661600-49666000 | Weak transcription | Osteobl | bone |
7 | chr8:49661800-49665400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |