Variant report
Variant | rs4727933 |
---|---|
Chromosome Location | chr7:121163728-121163729 |
allele | C/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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10228676 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10233243 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10237611 | 0.92[ASN][1000 genomes] |
rs10240973 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10253256 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10258260 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10258506 | 0.87[ASN][1000 genomes] |
rs10258640 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10259325 | 0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10270561 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10480752 | 0.92[ASN][1000 genomes] |
rs10953936 | 0.84[ASN][1000 genomes] |
rs10953937 | 0.80[ASN][1000 genomes] |
rs11761290 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1206560 | 0.87[ASN][1000 genomes] |
rs12535189 | 0.83[AFR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12540408 | 0.94[ASN][1000 genomes] |
rs12706358 | 0.84[ASN][1000 genomes] |
rs13229583 | 0.92[ASN][1000 genomes] |
rs1406194 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1528352 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1881374 | 0.90[ASN][1000 genomes] |
rs1881375 | 0.87[ASN][1000 genomes] |
rs1881376 | 0.87[ASN][1000 genomes] |
rs1919086 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1983493 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1983494 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1983495 | 0.87[ASN][1000 genomes] |
rs1983496 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2049702 | 0.87[ASN][1000 genomes] |
rs2103298 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2103299 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2141364 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2178188 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs28485397 | 0.94[ASN][1000 genomes] |
rs28578522 | 0.94[ASN][1000 genomes] |
rs28696257 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs34843814 | 0.83[ASN][1000 genomes] |
rs3847091 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3847092 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3857836 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4145963 | 0.89[ASN][1000 genomes] |
rs4731023 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4731024 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4731025 | 0.87[ASN][1000 genomes] |
rs5000114 | 0.88[ASN][1000 genomes] |
rs6953922 | 0.90[ASN][1000 genomes] |
rs6954048 | 0.83[ASN][1000 genomes] |
rs6960065 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7777295 | 0.87[ASN][1000 genomes] |
rs7777787 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7787312 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7791746 | 0.87[ASN][1000 genomes] |
rs7793736 | 0.98[ASN][1000 genomes] |
rs7795140 | 0.94[ASN][1000 genomes] |
rs867706 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9649443 | 0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9719308 | 0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9719756 | 0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9719758 | 0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1025430 | chr7:120638930-121179289 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
2 | nsv1026322 | chr7:120841937-121188037 | Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
3 | nsv539102 | chr7:120841937-121188037 | Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
4 | nsv1032054 | chr7:120926379-121432971 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
5 | nsv539103 | chr7:120926379-121432971 | Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
6 | nsv428507 | chr7:121037303-121191934 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
7 | nsv608333 | chr7:121132213-121379616 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv1015438 | chr7:121161554-121221761 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
9 | nsv824290 | chr7:121161692-121179342 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
10 | nsv824291 | chr7:121161896-121179567 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
11 | esv1811558 | chr7:121161987-121186293 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
12 | nsv442067 | chr7:121161987-121186293 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:121160800-121165000 | Weak transcription | Osteobl | bone |
2 | chr7:121160800-121165200 | Weak transcription | Adipose Nuclei | Adipose |
3 | chr7:121161200-121165000 | Weak transcription | NHDF-Ad | bronchial |
4 | chr7:121162200-121164800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
5 | chr7:121162400-121164400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
6 | chr7:121162400-121165200 | Weak transcription | Colon Smooth Muscle | Colon |
7 | chr7:121162400-121165200 | Weak transcription | Rectal Smooth Muscle | rectum |
8 | chr7:121162400-121168600 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
9 | chr7:121162800-121170400 | Weak transcription | Fetal Brain Male | brain |
10 | chr7:121163600-121165200 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |