Variant report
Variant | rs4696999 |
---|---|
Chromosome Location | chr4:22028976-22028977 |
allele | C/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 | chr4:22028111..22029824-chr4:22035660..22037244,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10433826 | 0.87[EUR][1000 genomes] |
rs12501816 | 0.86[EUR][1000 genomes] |
rs13108588 | 0.92[EUR][1000 genomes] |
rs13132801 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1513563 | 0.83[YRI][hapmap] |
rs1513574 | 0.91[EUR][1000 genomes] |
rs17526294 | 0.86[EUR][1000 genomes] |
rs2015779 | 0.94[EUR][1000 genomes] |
rs34196510 | 0.94[EUR][1000 genomes] |
rs34512134 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34843622 | 0.94[EUR][1000 genomes] |
rs34927464 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4697263 | 0.86[EUR][1000 genomes] |
rs67235125 | 0.86[EUR][1000 genomes] |
rs68147450 | 0.83[AFR][1000 genomes];0.98[EUR][1000 genomes] |
rs6833673 | 0.94[EUR][1000 genomes] |
rs6834048 | 0.84[AFR][1000 genomes] |
rs6839252 | 0.94[EUR][1000 genomes] |
rs7659568 | 0.94[EUR][1000 genomes] |
rs925570 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817467 | chr4:21602921-22422816 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv432584 | chr4:22009677-22080362 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | esv2757925 | chr4:22011581-22230718 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2759232 | chr4:22011581-22230718 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | esv2757043 | chr4:22017167-22090982 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
6 | nsv432585 | chr4:22017218-22070731 | Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
7 | nsv435775 | chr4:22026385-22032731 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:22028800-22029000 | ZNF genes & repeats | H9 Cell Line | embryonic stem cell |