Variant report
Variant | rs11813823 |
---|---|
Chromosome Location | chr10:45157941-45157942 |
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] |
---|---|
rs10900108 | 1.00[ASN][1000 genomes] |
rs10900114 | 1.00[ASN][1000 genomes] |
rs10900115 | 1.00[ASN][1000 genomes] |
rs10900116 | 1.00[ASN][1000 genomes] |
rs10900117 | 1.00[ASN][1000 genomes] |
rs10900118 | 1.00[ASN][1000 genomes] |
rs10900119 | 1.00[ASN][1000 genomes] |
rs11239199 | 1.00[ASN][1000 genomes] |
rs11239239 | 1.00[ASN][1000 genomes] |
rs11239240 | 1.00[ASN][1000 genomes] |
rs11239242 | 1.00[ASN][1000 genomes] |
rs11239245 | 1.00[ASN][1000 genomes] |
rs11239246 | 1.00[ASN][1000 genomes] |
rs11239248 | 1.00[ASN][1000 genomes] |
rs11239251 | 1.00[ASN][1000 genomes] |
rs11239254 | 1.00[ASN][1000 genomes] |
rs11239255 | 1.00[ASN][1000 genomes] |
rs11239256 | 1.00[ASN][1000 genomes] |
rs11239258 | 1.00[ASN][1000 genomes] |
rs11239259 | 1.00[ASN][1000 genomes] |
rs11239263 | 1.00[ASN][1000 genomes] |
rs11239264 | 1.00[ASN][1000 genomes] |
rs11591579 | 1.00[ASN][1000 genomes] |
rs11592342 | 1.00[ASN][1000 genomes] |
rs11593530 | 1.00[ASN][1000 genomes] |
rs11595568 | 1.00[ASN][1000 genomes] |
rs11596087 | 1.00[ASN][1000 genomes] |
rs11596156 | 1.00[ASN][1000 genomes] |
rs11596531 | 1.00[ASN][1000 genomes] |
rs11596589 | 1.00[ASN][1000 genomes] |
rs11596593 | 1.00[ASN][1000 genomes] |
rs11597029 | 1.00[ASN][1000 genomes] |
rs11597131 | 1.00[ASN][1000 genomes] |
rs11598037 | 1.00[ASN][1000 genomes] |
rs11598421 | 1.00[ASN][1000 genomes] |
rs11598433 | 1.00[ASN][1000 genomes] |
rs11598611 | 1.00[ASN][1000 genomes] |
rs11598612 | 1.00[ASN][1000 genomes] |
rs11598952 | 1.00[ASN][1000 genomes] |
rs11812151 | 1.00[ASN][1000 genomes] |
rs11812387 | 1.00[ASN][1000 genomes] |
rs11813028 | 1.00[ASN][1000 genomes] |
rs11813782 | 1.00[ASN][1000 genomes] |
rs11815268 | 1.00[ASN][1000 genomes] |
rs11815663 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11817455 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11818158 | 1.00[ASN][1000 genomes] |
rs11818379 | 1.00[ASN][1000 genomes] |
rs11819599 | 0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs11819624 | 1.00[ASN][1000 genomes] |
rs11819716 | 1.00[ASN][1000 genomes] |
rs12146205 | 1.00[ASN][1000 genomes] |
rs12357368 | 1.00[ASN][1000 genomes] |
rs1253325 | 1.00[ASN][1000 genomes] |
rs1325160 | 1.00[ASN][1000 genomes] |
rs1383373 | 1.00[ASN][1000 genomes] |
rs1480596 | 1.00[ASN][1000 genomes] |
rs1480597 | 1.00[ASN][1000 genomes] |
rs1480598 | 1.00[ASN][1000 genomes] |
rs1590559 | 1.00[ASN][1000 genomes] |
rs1600615 | 1.00[ASN][1000 genomes] |
rs17157056 | 1.00[ASN][1000 genomes] |
rs17410010 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17410452 | 1.00[ASN][1000 genomes] |
rs17411047 | 1.00[ASN][1000 genomes] |
rs17411958 | 1.00[ASN][1000 genomes] |
rs17414426 | 1.00[ASN][1000 genomes] |
rs17488358 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1749325 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1749327 | 1.00[ASN][1000 genomes] |
rs1749331 | 1.00[ASN][1000 genomes] |
rs1749333 | 1.00[ASN][1000 genomes] |
rs17501987 | 1.00[ASN][1000 genomes] |
rs17502111 | 1.00[ASN][1000 genomes] |
rs17502384 | 1.00[ASN][1000 genomes] |
rs17502724 | 1.00[ASN][1000 genomes] |
rs1771981 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1771985 | 1.00[ASN][1000 genomes] |
rs1771990 | 1.00[ASN][1000 genomes] |
rs1771996 | 1.00[ASN][1000 genomes] |
rs1771999 | 1.00[ASN][1000 genomes] |
rs1831671 | 1.00[ASN][1000 genomes] |
rs1947860 | 1.00[ASN][1000 genomes] |
rs1977325 | 1.00[ASN][1000 genomes] |
rs1977326 | 1.00[ASN][1000 genomes] |
rs1994003 | 1.00[ASN][1000 genomes] |
rs2069045 | 1.00[ASN][1000 genomes] |
rs2086420 | 1.00[ASN][1000 genomes] |
rs2094018 | 1.00[ASN][1000 genomes] |
rs2477528 | 1.00[ASN][1000 genomes] |
rs2477529 | 1.00[ASN][1000 genomes] |
rs2611373 | 1.00[ASN][1000 genomes] |
rs2611374 | 1.00[ASN][1000 genomes] |
rs2611375 | 1.00[ASN][1000 genomes] |
rs2764349 | 1.00[ASN][1000 genomes] |
rs2764350 | 1.00[ASN][1000 genomes] |
rs2764351 | 1.00[ASN][1000 genomes] |
rs2764361 | 1.00[ASN][1000 genomes] |
rs2793295 | 1.00[ASN][1000 genomes] |
rs2793297 | 1.00[ASN][1000 genomes] |
rs2793298 | 1.00[ASN][1000 genomes] |
rs2793299 | 1.00[ASN][1000 genomes] |
rs2793301 | 1.00[ASN][1000 genomes] |
rs2793305 | 1.00[ASN][1000 genomes] |
rs2793308 | 1.00[ASN][1000 genomes] |
rs2793311 | 1.00[ASN][1000 genomes] |
rs2793312 | 1.00[CHB][hapmap] |
rs34660870 | 1.00[ASN][1000 genomes] |
rs35250498 | 1.00[ASN][1000 genomes] |
rs35363088 | 1.00[ASN][1000 genomes] |
rs3890283 | 1.00[ASN][1000 genomes] |
rs4035631 | 1.00[ASN][1000 genomes] |
rs4268462 | 1.00[ASN][1000 genomes] |
rs4356177 | 1.00[ASN][1000 genomes] |
rs4362097 | 1.00[ASN][1000 genomes] |
rs4362098 | 1.00[ASN][1000 genomes] |
rs4363543 | 1.00[ASN][1000 genomes] |
rs4363544 | 1.00[ASN][1000 genomes] |
rs74138464 | 1.00[ASN][1000 genomes] |
rs7901009 | 1.00[ASN][1000 genomes] |
rs7911712 | 1.00[ASN][1000 genomes] |
rs7912668 | 1.00[ASN][1000 genomes] |
rs967989 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2422287 | chr10:45044161-45257684 | Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv831843 | chr10:45084703-45280032 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | esv3373331 | chr10:45156246-45160444 | Weak transcription Enhancers Bivalent Enhancer | n/a | n/a | inside rSNPs | n/a |
4 | esv2584008 | chr10:45157495-45159150 | Bivalent Enhancer Enhancers Weak transcription | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:45154800-45158000 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
2 | chr10:45155000-45159600 | Enhancers | Fetal Muscle Leg | muscle |
3 | chr10:45156200-45158000 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr10:45156400-45161600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
5 | chr10:45156400-45175800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
6 | chr10:45157000-45158000 | Enhancers | Fetal Stomach | stomach |
7 | chr10:45157200-45158000 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
8 | chr10:45157200-45158000 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
9 | chr10:45157200-45158000 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin02 | Skin |
10 | chr10:45157200-45159000 | Enhancers | Fetal Muscle Trunk | muscle |
11 | chr10:45157400-45162200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
12 | chr10:45157800-45158000 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
13 | chr10:45157800-45158000 | Enhancers | Muscle Satellite Cultured Cells | -- |
14 | chr10:45157800-45158000 | Enhancers | NHLF | lung |