Variant report
Variant | rs17145154 |
---|---|
Chromosome Location | chr7:21777455-21777456 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10156149 | 1.00[CEU][hapmap] |
rs10261104 | 1.00[ASW][hapmap] |
rs12672447 | 1.00[CEU][hapmap] |
rs16872905 | 1.00[CEU][hapmap] |
rs16872969 | 1.00[ASW][hapmap] |
rs17145200 | 1.00[CEU][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.84[ASN][1000 genomes] |
rs17145214 | 1.00[CEU][hapmap];0.81[ASN][1000 genomes] |
rs17145249 | 1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.80[ASN][1000 genomes] |
rs17145261 | 1.00[CEU][hapmap] |
rs17145274 | 1.00[CEU][hapmap] |
rs17354984 | 1.00[CEU][hapmap] |
rs2072222 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap] |
rs2965362 | 1.00[CEU][hapmap] |
rs2965363 | 1.00[CEU][hapmap] |
rs56881851 | 0.80[ASN][1000 genomes] |
rs67536067 | 0.83[ASN][1000 genomes] |
rs7796262 | 1.00[CEU][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1018133 | chr7:21740118-22055283 | Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv1016063 | chr7:21740433-21808410 | Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |