Variant report
Variant | rs71522551 |
---|---|
Chromosome Location | chr8:130675173-130675174 |
allele | A/G |
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 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000229140 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10097823 | 0.82[ASN][1000 genomes] |
rs10098045 | 0.82[ASN][1000 genomes] |
rs12155665 | 0.88[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs12544799 | 0.94[ASN][1000 genomes] |
rs12545821 | 0.89[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs13249422 | 0.95[ASN][1000 genomes] |
rs13249717 | 0.93[ASN][1000 genomes] |
rs13250002 | 0.93[ASN][1000 genomes] |
rs13250085 | 0.82[ASN][1000 genomes] |
rs13252239 | 0.92[ASN][1000 genomes] |
rs13256078 | 0.83[ASN][1000 genomes] |
rs13258791 | 0.93[ASN][1000 genomes] |
rs13267723 | 0.82[EUR][1000 genomes] |
rs16904128 | 0.81[ASN][1000 genomes] |
rs16904136 | 0.94[ASN][1000 genomes] |
rs16904138 | 0.94[ASN][1000 genomes] |
rs16904139 | 0.94[ASN][1000 genomes] |
rs28408379 | 0.82[ASN][1000 genomes] |
rs28491539 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs34064664 | 0.83[ASN][1000 genomes] |
rs34135752 | 0.87[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs34271371 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34325696 | 0.89[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs34389024 | 0.90[ASN][1000 genomes] |
rs35057631 | 0.93[ASN][1000 genomes] |
rs35319444 | 0.82[ASN][1000 genomes] |
rs35406957 | 0.82[ASN][1000 genomes] |
rs35484532 | 0.83[ASN][1000 genomes] |
rs35823317 | 0.83[ASN][1000 genomes] |
rs35928814 | 0.85[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs36121385 | 0.82[ASN][1000 genomes] |
rs4327829 | 0.84[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4397369 | 0.82[ASN][1000 genomes] |
rs4397370 | 0.81[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4448234 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4518628 | 0.84[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4562281 | 0.91[ASN][1000 genomes] |
rs4565426 | 0.83[ASN][1000 genomes] |
rs4566996 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs4609165 | 0.91[ASN][1000 genomes] |
rs4626563 | 0.94[ASN][1000 genomes] |
rs4634602 | 0.80[ASN][1000 genomes] |
rs4733553 | 0.92[ASN][1000 genomes] |
rs4733556 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs4733720 | 0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs58311093 | 0.94[ASN][1000 genomes] |
rs6470753 | 0.89[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6985166 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs6991709 | 0.85[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs6991966 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs6997969 | 0.94[ASN][1000 genomes] |
rs6998156 | 0.94[ASN][1000 genomes] |
rs6998279 | 0.94[ASN][1000 genomes] |
rs6998547 | 0.94[ASN][1000 genomes] |
rs6998877 | 0.93[ASN][1000 genomes] |
rs7006026 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7006796 | 0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7812657 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs7828331 | 0.81[ASN][1000 genomes] |
rs7841900 | 0.83[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs7841975 | 0.92[ASN][1000 genomes] |
rs9792140 | 0.81[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs9792265 | 0.81[AMR][1000 genomes];0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv891446 | chr8:130656205-130710638 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:130672800-130675800 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr8:130674000-130675600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
3 | chr8:130674000-130675800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
4 | chr8:130674000-130677800 | Weak transcription | K562 | blood |
5 | chr8:130675000-130676400 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |