Variant report
Variant | rs12062568 |
---|---|
Chromosome Location | chr1:102118136-102118137 |
allele | A/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 | chr1:102116557..102119027-chr1:102123747..102125780,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11800181 | 0.99[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11802784 | 1.00[ASN][1000 genomes] |
rs12062937 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12079191 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1601235 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2086852 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4907945 | 1.00[ASN][1000 genomes] |
rs4907946 | 1.00[ASN][1000 genomes] |
rs4907948 | 1.00[ASN][1000 genomes] |
rs4907950 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4908169 | 1.00[ASN][1000 genomes] |
rs56064810 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56140505 | 1.00[ASN][1000 genomes] |
rs56173817 | 0.81[EUR][1000 genomes] |
rs56221742 | 0.90[EUR][1000 genomes] |
rs56807681 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57544888 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60629450 | 0.82[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6660076 | 0.95[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6679807 | 0.80[AFR][1000 genomes];0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv870459 | chr1:102112168-102166616 | Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:102118000-102122600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |