Variant report
Variant | rs7026450 |
---|---|
Chromosome Location | chr9:115666976-115666977 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr9:115606178..115608888-chr9:115665655..115667772,2 | K562 | blood: | |
2 | chr9:115661009..115663181-chr9:115664939..115667779,3 | MCF-7 | breast: | |
3 | chr9:115658787..115660468-chr9:115666043..115668753,2 | K562 | blood: | |
4 | chr9:115665975..115668573-chr9:115679220..115680887,2 | K562 | blood: | |
5 | chr9:115665727..115668117-chr9:115679003..115681024,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10115711 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10124260 | 1.00[ASN][1000 genomes] |
rs10124939 | 0.96[EUR][1000 genomes] |
rs10124979 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10733594 | 1.00[ASN][1000 genomes] |
rs10733598 | 1.00[ASN][1000 genomes] |
rs10733599 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10739370 | 1.00[ASN][1000 genomes] |
rs10739373 | 1.00[ASN][1000 genomes] |
rs10739374 | 1.00[ASN][1000 genomes] |
rs10739376 | 1.00[ASN][1000 genomes] |
rs10739380 | 0.96[EUR][1000 genomes] |
rs10759590 | 1.00[ASN][1000 genomes] |
rs10759603 | 1.00[ASN][1000 genomes] |
rs10759604 | 1.00[ASN][1000 genomes] |
rs1158331 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1324931 | 1.00[ASN][1000 genomes] |
rs1418409 | 1.00[ASN][1000 genomes] |
rs1539338 | 1.00[ASN][1000 genomes] |
rs1570754 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1693411 | 1.00[ASN][1000 genomes] |
rs1711746 | 1.00[ASN][1000 genomes] |
rs1711747 | 1.00[ASN][1000 genomes] |
rs1832890 | 1.00[ASN][1000 genomes] |
rs1891402 | 1.00[ASN][1000 genomes] |
rs2025544 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2051018 | 1.00[ASN][1000 genomes] |
rs2147643 | 1.00[ASN][1000 genomes] |
rs2147646 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2153837 | 1.00[ASN][1000 genomes] |
rs2182048 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2185769 | 1.00[ASN][1000 genomes] |
rs2645985 | 1.00[ASN][1000 genomes] |
rs2645994 | 1.00[ASN][1000 genomes] |
rs2796025 | 1.00[ASN][1000 genomes] |
rs2796028 | 1.00[ASN][1000 genomes] |
rs2796031 | 1.00[ASN][1000 genomes] |
rs2796035 | 1.00[ASN][1000 genomes] |
rs4246892 | 1.00[ASN][1000 genomes] |
rs4360356 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4549852 | 1.00[ASN][1000 genomes] |
rs4978507 | 1.00[ASN][1000 genomes] |
rs4978510 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4978511 | 0.96[EUR][1000 genomes] |
rs4979154 | 1.00[ASN][1000 genomes] |
rs4979155 | 1.00[ASN][1000 genomes] |
rs4979157 | 1.00[ASN][1000 genomes] |
rs4979165 | 1.00[ASN][1000 genomes] |
rs4979183 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4979184 | 0.97[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4979186 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6477959 | 1.00[ASN][1000 genomes] |
rs700122 | 1.00[ASN][1000 genomes] |
rs7030795 | 1.00[ASN][1000 genomes] |
rs7038684 | 1.00[ASN][1000 genomes] |
rs7040954 | 0.97[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7041965 | 1.00[ASN][1000 genomes] |
rs7047914 | 1.00[ASN][1000 genomes] |
rs7859175 | 1.00[ASN][1000 genomes] |
rs7869100 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs786961 | 1.00[ASN][1000 genomes] |
rs786965 | 1.00[ASN][1000 genomes] |
rs786966 | 1.00[ASN][1000 genomes] |
rs786967 | 1.00[ASN][1000 genomes] |
rs786968 | 1.00[ASN][1000 genomes] |
rs786969 | 1.00[ASN][1000 genomes] |
rs786972 | 1.00[ASN][1000 genomes] |
rs786973 | 1.00[ASN][1000 genomes] |
rs786977 | 1.00[ASN][1000 genomes] |
rs7872628 | 1.00[ASN][1000 genomes] |
rs787278 | 1.00[ASN][1000 genomes] |
rs787281 | 1.00[ASN][1000 genomes] |
rs787285 | 1.00[ASN][1000 genomes] |
rs787286 | 1.00[ASN][1000 genomes] |
rs787287 | 1.00[ASN][1000 genomes] |
rs787291 | 1.00[ASN][1000 genomes] |
rs787296 | 1.00[ASN][1000 genomes] |
rs787299 | 1.00[ASN][1000 genomes] |
rs787302 | 1.00[ASN][1000 genomes] |
rs787303 | 1.00[ASN][1000 genomes] |
rs7873289 | 1.00[ASN][1000 genomes] |
rs885387 | 1.00[ASN][1000 genomes] |
rs912662 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs947609 | 1.00[ASN][1000 genomes] |
rs980345 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758198 | chr9:115240454-116002951 | Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | diseases |
2 | esv2759710 | chr9:115240454-116002951 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | diseases |
3 | nsv893733 | chr9:115397206-115712068 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
4 | nsv1047000 | chr9:115610445-115884038 | ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:115661600-115667000 | Weak transcription | Fetal Kidney | kidney |
2 | chr9:115665800-115667400 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
3 | chr9:115665800-115682000 | Weak transcription | Right Atrium | heart |
4 | chr9:115666000-115667000 | Weak transcription | HepG2 | liver |