Variant report
Variant | rs17075422 |
---|---|
Chromosome Location | chr3:43308315-43308316 |
allele | A/G |
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 | chr3:43306571..43309448-chr3:43310200..43312609,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs17075424 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17075519 | 1.00[AMR][1000 genomes] |
rs17075525 | 1.00[AMR][1000 genomes] |
rs17075540 | 1.00[AMR][1000 genomes] |
rs17075545 | 1.00[AMR][1000 genomes] |
rs17075555 | 1.00[AMR][1000 genomes] |
rs17075561 | 1.00[AMR][1000 genomes] |
rs17075563 | 1.00[AMR][1000 genomes] |
rs17075568 | 1.00[AMR][1000 genomes] |
rs17075570 | 1.00[AMR][1000 genomes] |
rs17075574 | 1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes] |
rs17075581 | 1.00[ASW][hapmap];0.88[LWK][hapmap];1.00[MKK][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17075587 | 1.00[AMR][1000 genomes] |
rs17075614 | 1.00[AMR][1000 genomes] |
rs17075617 | 1.00[AMR][1000 genomes] |
rs17075623 | 1.00[AMR][1000 genomes] |
rs17075624 | 1.00[AMR][1000 genomes] |
rs17254716 | 1.00[AMR][1000 genomes] |
rs17320381 | 1.00[AMR][1000 genomes] |
rs17405728 | 1.00[AMR][1000 genomes] |
rs17406148 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17406718 | 1.00[ASW][hapmap];1.00[MKK][hapmap] |
rs17472888 | 1.00[AMR][1000 genomes] |
rs34343482 | 1.00[AMR][1000 genomes] |
rs34730190 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs41321344 | 1.00[AMR][1000 genomes] |
rs55694436 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55727302 | 1.00[AMR][1000 genomes] |
rs55730605 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55760455 | 1.00[AMR][1000 genomes] |
rs55765643 | 1.00[AMR][1000 genomes] |
rs55804512 | 1.00[AMR][1000 genomes] |
rs55837468 | 1.00[AMR][1000 genomes] |
rs55864645 | 1.00[AMR][1000 genomes] |
rs55887904 | 1.00[AMR][1000 genomes] |
rs55908419 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55915337 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs55951861 | 1.00[AMR][1000 genomes] |
rs55957435 | 1.00[AMR][1000 genomes] |
rs56100043 | 1.00[AMR][1000 genomes] |
rs56225070 | 1.00[AMR][1000 genomes] |
rs56282728 | 1.00[AMR][1000 genomes] |
rs56285372 | 1.00[AMR][1000 genomes] |
rs56286131 | 1.00[AMR][1000 genomes] |
rs56388016 | 1.00[AMR][1000 genomes] |
rs56395291 | 1.00[AMR][1000 genomes] |
rs56659864 | 1.00[AMR][1000 genomes] |
rs56741341 | 1.00[AMR][1000 genomes] |
rs57019763 | 1.00[AMR][1000 genomes] |
rs57020473 | 1.00[AMR][1000 genomes] |
rs57376786 | 1.00[AMR][1000 genomes] |
rs58158782 | 1.00[AMR][1000 genomes] |
rs58209397 | 1.00[AMR][1000 genomes] |
rs58216554 | 1.00[AMR][1000 genomes] |
rs58508138 | 1.00[AMR][1000 genomes] |
rs58636339 | 1.00[AMR][1000 genomes] |
rs58866653 | 1.00[AMR][1000 genomes] |
rs59113361 | 1.00[AMR][1000 genomes] |
rs59121457 | 1.00[AMR][1000 genomes] |
rs59276993 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59495244 | 1.00[AMR][1000 genomes] |
rs59545985 | 1.00[AMR][1000 genomes] |
rs59706458 | 1.00[AMR][1000 genomes] |
rs59872395 | 1.00[AMR][1000 genomes] |
rs59930267 | 1.00[AMR][1000 genomes] |
rs60689590 | 1.00[AMR][1000 genomes] |
rs61270592 | 1.00[AMR][1000 genomes] |
rs61375879 | 1.00[AMR][1000 genomes] |
rs61644103 | 1.00[AMR][1000 genomes] |
rs73829182 | 1.00[AMR][1000 genomes] |
rs73829183 | 1.00[AMR][1000 genomes] |
rs73829189 | 1.00[AMR][1000 genomes] |
rs73829191 | 1.00[AMR][1000 genomes] |
rs73831214 | 1.00[AMR][1000 genomes] |
rs73831218 | 1.00[AMR][1000 genomes] |
rs73831224 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73831226 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73831227 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73831230 | 0.81[AFR][1000 genomes] |
rs73831232 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73831233 | 1.00[AMR][1000 genomes] |
rs73831234 | 1.00[AMR][1000 genomes] |
rs73831236 | 1.00[AMR][1000 genomes] |
rs73831237 | 1.00[AMR][1000 genomes] |
rs73831238 | 1.00[AMR][1000 genomes] |
rs73831239 | 1.00[AMR][1000 genomes] |
rs73831240 | 1.00[AMR][1000 genomes] |
rs73831241 | 1.00[AMR][1000 genomes] |
rs73831242 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73831243 | 1.00[AMR][1000 genomes] |
rs73831244 | 1.00[AMR][1000 genomes] |
rs73831245 | 1.00[AMR][1000 genomes] |
rs73831247 | 1.00[AMR][1000 genomes] |
rs73831248 | 1.00[AMR][1000 genomes] |
rs73831249 | 1.00[AMR][1000 genomes] |
rs73831250 | 1.00[AMR][1000 genomes] |
rs73831251 | 1.00[AMR][1000 genomes] |
rs73831252 | 1.00[AMR][1000 genomes] |
rs73831253 | 1.00[AMR][1000 genomes] |
rs73831256 | 1.00[AMR][1000 genomes] |
rs73831261 | 1.00[AMR][1000 genomes] |
rs73831271 | 1.00[AMR][1000 genomes] |
rs73831273 | 1.00[AMR][1000 genomes] |
rs73831274 | 1.00[AMR][1000 genomes] |
rs73831275 | 1.00[AMR][1000 genomes] |
rs73831277 | 1.00[AMR][1000 genomes] |
rs73831279 | 1.00[AMR][1000 genomes] |
rs73831280 | 1.00[AMR][1000 genomes] |
rs73831281 | 1.00[AMR][1000 genomes] |
rs73831283 | 1.00[AMR][1000 genomes] |
rs73831285 | 1.00[AMR][1000 genomes] |
rs984347 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752008 | chr3:43285369-43360879 | Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv1009102 | chr3:43285369-43369712 | Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:43302000-43314000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr3:43302400-43310000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |