Variant report
Variant | rs1160101 |
---|---|
Chromosome Location | chr3:110475055-110475056 |
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 |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1020891 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1037960 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1040004 | 1.00[EUR][1000 genomes] |
rs11929276 | 1.00[EUR][1000 genomes] |
rs12330541 | 1.00[EUR][1000 genomes] |
rs1350928 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1350931 | 1.00[EUR][1000 genomes] |
rs1381827 | 1.00[EUR][1000 genomes] |
rs1381829 | 1.00[EUR][1000 genomes] |
rs1398343 | 1.00[EUR][1000 genomes] |
rs1462297 | 1.00[EUR][1000 genomes] |
rs1462312 | 1.00[EUR][1000 genomes] |
rs1462791 | 1.00[EUR][1000 genomes] |
rs1462792 | 1.00[EUR][1000 genomes] |
rs1462796 | 1.00[EUR][1000 genomes] |
rs1462806 | 1.00[EUR][1000 genomes] |
rs1512513 | 1.00[EUR][1000 genomes] |
rs1512517 | 1.00[EUR][1000 genomes] |
rs1533193 | 1.00[EUR][1000 genomes] |
rs1546533 | 1.00[EUR][1000 genomes] |
rs1580287 | 1.00[EUR][1000 genomes] |
rs1599575 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1599577 | 1.00[EUR][1000 genomes] |
rs1599665 | 1.00[EUR][1000 genomes] |
rs1841734 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1849369 | 1.00[EUR][1000 genomes] |
rs1903758 | 1.00[EUR][1000 genomes] |
rs1913098 | 1.00[EUR][1000 genomes] |
rs1960628 | 1.00[EUR][1000 genomes] |
rs1975901 | 1.00[EUR][1000 genomes] |
rs1993781 | 1.00[EUR][1000 genomes] |
rs1993801 | 1.00[EUR][1000 genomes] |
rs2036968 | 1.00[EUR][1000 genomes] |
rs2054376 | 1.00[EUR][1000 genomes] |
rs2061682 | 1.00[EUR][1000 genomes] |
rs2137383 | 1.00[EUR][1000 genomes] |
rs2169566 | 1.00[EUR][1000 genomes] |
rs3957571 | 1.00[EUR][1000 genomes] |
rs3957572 | 1.00[EUR][1000 genomes] |
rs4305447 | 1.00[EUR][1000 genomes] |
rs4333116 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs4549301 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs4593059 | 1.00[EUR][1000 genomes] |
rs4682012 | 1.00[EUR][1000 genomes] |
rs4682021 | 1.00[EUR][1000 genomes] |
rs4682216 | 1.00[EUR][1000 genomes] |
rs4682218 | 1.00[EUR][1000 genomes] |
rs4682220 | 1.00[EUR][1000 genomes] |
rs58412853 | 1.00[EUR][1000 genomes] |
rs6437932 | 1.00[EUR][1000 genomes] |
rs6437935 | 1.00[EUR][1000 genomes] |
rs6437936 | 1.00[EUR][1000 genomes] |
rs6766908 | 1.00[EUR][1000 genomes] |
rs6780526 | 1.00[EUR][1000 genomes] |
rs6781418 | 1.00[EUR][1000 genomes] |
rs6781884 | 1.00[EUR][1000 genomes] |
rs6794368 | 1.00[EUR][1000 genomes] |
rs6798353 | 1.00[EUR][1000 genomes] |
rs72941202 | 1.00[EUR][1000 genomes] |
rs72943104 | 1.00[EUR][1000 genomes] |
rs72943107 | 1.00[EUR][1000 genomes] |
rs72943108 | 1.00[EUR][1000 genomes] |
rs72943110 | 1.00[EUR][1000 genomes] |
rs72943111 | 1.00[EUR][1000 genomes] |
rs72943114 | 1.00[EUR][1000 genomes] |
rs72943119 | 1.00[EUR][1000 genomes] |
rs72944942 | 1.00[EUR][1000 genomes] |
rs72944943 | 1.00[EUR][1000 genomes] |
rs72944949 | 1.00[EUR][1000 genomes] |
rs72944956 | 1.00[EUR][1000 genomes] |
rs72944965 | 1.00[EUR][1000 genomes] |
rs7609772 | 1.00[EUR][1000 genomes] |
rs7612471 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7615275 | 1.00[EUR][1000 genomes] |
rs7618482 | 0.91[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7619978 | 1.00[EUR][1000 genomes] |
rs7634788 | 1.00[EUR][1000 genomes] |
rs7639735 | 1.00[EUR][1000 genomes] |
rs7641366 | 1.00[EUR][1000 genomes] |
rs7642037 | 1.00[EUR][1000 genomes] |
rs7644614 | 1.00[EUR][1000 genomes] |
rs9288915 | 1.00[EUR][1000 genomes] |
rs931024 | 1.00[EUR][1000 genomes] |
rs964444 | 1.00[EUR][1000 genomes] |
rs9818867 | 1.00[EUR][1000 genomes] |
rs9823218 | 1.00[EUR][1000 genomes] |
rs9824638 | 1.00[EUR][1000 genomes] |
rs9826523 | 1.00[EUR][1000 genomes] |
rs9829084 | 1.00[EUR][1000 genomes] |
rs9830162 | 1.00[EUR][1000 genomes] |
rs9856917 | 1.00[EUR][1000 genomes] |
rs9860353 | 1.00[EUR][1000 genomes] |
rs9868966 | 1.00[EUR][1000 genomes] |
rs9869379 | 1.00[EUR][1000 genomes] |
rs9874159 | 1.00[EUR][1000 genomes] |
rs988374 | 1.00[EUR][1000 genomes] |
rs992130 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001810 | chr3:110158316-110522247 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1010230 | chr3:110204439-110588814 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv536688 | chr3:110204439-110588814 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1011034 | chr3:110209344-110559021 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv536689 | chr3:110209344-110559021 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv1003106 | chr3:110264476-111105943 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
7 | nsv1014199 | chr3:110293896-110754155 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | nsv829673 | chr3:110378069-110530815 | Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:110471400-110492200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr3:110472400-110475400 | Enhancers | HUES48 Cell Line | embryonic stem cell |
3 | chr3:110472600-110492400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr3:110472800-110475600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
5 | chr3:110473000-110475200 | Enhancers | HepG2 | liver |
6 | chr3:110473000-110475800 | Enhancers | HUES64 Cell Line | embryonic stem cell |
7 | chr3:110473200-110475800 | Enhancers | H1 Cell Line | embryonic stem cell |
8 | chr3:110473200-110476200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
9 | chr3:110473400-110475200 | Enhancers | H9 Cell Line | embryonic stem cell |
10 | chr3:110473400-110475200 | Enhancers | Fetal Muscle Leg | muscle |
11 | chr3:110473600-110475400 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
12 | chr3:110475000-110475600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |