Variant report
| Variant | rs72908944 |
|---|---|
| Chromosome Location | chr4:99911915-99911916 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:6)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:6 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr4:99849065..99851957-chr4:99908579..99912810,4 | K562 | blood: | |
| 2 | chr4:99906747..99909134-chr4:99909881..99912158,2 | MCF-7 | breast: | |
| 3 | chr4:99848849..99850421-chr4:99911434..99914059,2 | MCF-7 | breast: | |
| 4 | chr4:99911236..99913090-chr4:99951415..99953852,2 | MCF-7 | breast: | |
| 5 | chr4:99911434..99913629-chr4:99914633..99918539,3 | K562 | blood: | |
| 6 | chr4:99844460..99852883-chr4:99909835..99921707,41 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000238449 | Chromatin interaction |
| ENSG00000265213 | Chromatin interaction |
| ENSG00000164024 | Chromatin interaction |
| ENSG00000151247 | Chromatin interaction |
| ENSG00000263923 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:16)
| rs_ID | r2[population] |
|---|---|
| rs17028338 | 0.87[AFR][1000 genomes] |
| rs17028347 | 0.89[AFR][1000 genomes] |
| rs17028378 | 0.91[AFR][1000 genomes] |
| rs17028406 | 0.83[AFR][1000 genomes] |
| rs72908929 | 1.00[AFR][1000 genomes] |
| rs72908930 | 1.00[AFR][1000 genomes] |
| rs72908946 | 1.00[AFR][1000 genomes] |
| rs72908969 | 0.91[AFR][1000 genomes] |
| rs72908974 | 0.91[AFR][1000 genomes] |
| rs72908979 | 0.82[AFR][1000 genomes] |
| rs72908985 | 0.87[AFR][1000 genomes] |
| rs72908987 | 0.91[AFR][1000 genomes] |
| rs72909002 | 0.85[AFR][1000 genomes] |
| rs72910916 | 0.82[AFR][1000 genomes] |
| rs72910929 | 0.89[AFR][1000 genomes] |
| rs7678891 | 1.00[AFR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1009017 | chr4:99669441-100406394 | Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 57 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
