Variant report
Variant | rs1335195 |
---|---|
Chromosome Location | chr10:25877015-25877016 |
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 | chr10:25867129..25868995-chr10:25875572..25877987,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10508693 | 1.00[CHB][hapmap] |
rs12357174 | 1.00[CHB][hapmap] |
rs1335196 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes] |
rs1335197 | 1.00[CHB][hapmap] |
rs16926124 | 1.00[CHB][hapmap] |
rs16926153 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs16926158 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16926172 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17628278 | 1.00[CHB][hapmap] |
rs1981118 | 1.00[ASN][1000 genomes] |
rs2001385 | 1.00[EUR][1000 genomes] |
rs2026055 | 1.00[CHB][hapmap] |
rs4523593 | 1.00[CHB][hapmap] |
rs4747532 | 1.00[CHB][hapmap] |
rs6482497 | 1.00[CHB][hapmap] |
rs6482498 | 1.00[CHB][hapmap] |
rs6482499 | 1.00[CHB][hapmap] |
rs74124215 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7909167 | 0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7911892 | 1.00[CHB][hapmap] |
rs7921299 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3349863 | chr10:25614571-25946379 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv894972 | chr10:25849998-25917909 | Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:25876800-25884800 | Weak transcription | Cortex derived primary cultured neurospheres | brain |