Variant report
Variant | rs56132068 |
---|---|
Chromosome Location | chr11:36756686-36756687 |
allele | G/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] |
---|---|
rs10501159 | 0.85[EUR][1000 genomes] |
rs10501160 | 0.85[EUR][1000 genomes] |
rs10836580 | 0.85[EUR][1000 genomes] |
rs10836581 | 0.85[EUR][1000 genomes] |
rs11033708 | 0.85[EUR][1000 genomes] |
rs11033712 | 0.85[EUR][1000 genomes] |
rs11033717 | 0.85[EUR][1000 genomes] |
rs11033725 | 0.85[EUR][1000 genomes] |
rs11033727 | 0.85[EUR][1000 genomes] |
rs11033735 | 0.85[EUR][1000 genomes] |
rs11822918 | 0.83[EUR][1000 genomes] |
rs12279449 | 0.85[EUR][1000 genomes] |
rs12279924 | 0.85[EUR][1000 genomes] |
rs12286114 | 0.80[EUR][1000 genomes] |
rs12292943 | 0.85[EUR][1000 genomes] |
rs12293987 | 0.85[EUR][1000 genomes] |
rs12295400 | 0.85[EUR][1000 genomes] |
rs12416842 | 0.87[EUR][1000 genomes] |
rs12417057 | 0.87[EUR][1000 genomes] |
rs12417768 | 0.87[EUR][1000 genomes] |
rs12417778 | 0.87[EUR][1000 genomes] |
rs12417783 | 0.87[EUR][1000 genomes] |
rs12419750 | 0.87[EUR][1000 genomes] |
rs12420509 | 0.87[EUR][1000 genomes] |
rs12420930 | 0.87[EUR][1000 genomes] |
rs12420954 | 0.85[EUR][1000 genomes] |
rs12421512 | 0.87[EUR][1000 genomes] |
rs12421641 | 0.80[EUR][1000 genomes] |
rs1391542 | 0.87[EUR][1000 genomes] |
rs1391543 | 0.87[EUR][1000 genomes] |
rs1399600 | 0.80[EUR][1000 genomes] |
rs1498343 | 0.85[EUR][1000 genomes] |
rs1498344 | 0.85[EUR][1000 genomes] |
rs1515057 | 0.87[EUR][1000 genomes] |
rs16929067 | 0.81[EUR][1000 genomes] |
rs16929071 | 0.80[EUR][1000 genomes] |
rs16929076 | 0.80[EUR][1000 genomes] |
rs16929119 | 0.87[EUR][1000 genomes] |
rs16929136 | 0.85[EUR][1000 genomes] |
rs16929145 | 0.87[EUR][1000 genomes] |
rs16929147 | 0.87[EUR][1000 genomes] |
rs16929149 | 0.87[EUR][1000 genomes] |
rs16929170 | 0.87[EUR][1000 genomes] |
rs16929178 | 0.84[EUR][1000 genomes] |
rs16929182 | 0.85[EUR][1000 genomes] |
rs16929194 | 0.87[EUR][1000 genomes] |
rs16929197 | 0.87[EUR][1000 genomes] |
rs16929201 | 0.87[EUR][1000 genomes] |
rs16929204 | 0.87[EUR][1000 genomes] |
rs16929208 | 0.85[EUR][1000 genomes] |
rs16929216 | 0.87[EUR][1000 genomes] |
rs16929227 | 0.87[EUR][1000 genomes] |
rs16929247 | 0.85[EUR][1000 genomes] |
rs16929249 | 0.87[EUR][1000 genomes] |
rs2422296 | 0.85[EUR][1000 genomes] |
rs2422297 | 0.85[EUR][1000 genomes] |
rs34435837 | 0.85[EUR][1000 genomes] |
rs35329885 | 0.85[EUR][1000 genomes] |
rs3740957 | 0.87[EUR][1000 genomes] |
rs4151051 | 0.80[EUR][1000 genomes] |
rs57856061 | 0.85[EUR][1000 genomes] |
rs58084113 | 0.85[EUR][1000 genomes] |
rs59179248 | 0.85[EUR][1000 genomes] |
rs60281434 | 0.85[EUR][1000 genomes] |
rs61432856 | 0.85[EUR][1000 genomes] |
rs61686617 | 0.85[EUR][1000 genomes] |
rs7102491 | 0.87[EUR][1000 genomes] |
rs7102864 | 0.87[EUR][1000 genomes] |
rs7103064 | 0.85[EUR][1000 genomes] |
rs7110520 | 0.81[EUR][1000 genomes] |
rs7124815 | 0.85[EUR][1000 genomes] |
rs7125002 | 0.85[EUR][1000 genomes] |
rs7128419 | 0.85[EUR][1000 genomes] |
rs7130536 | 0.85[EUR][1000 genomes] |
rs7131496 | 0.85[EUR][1000 genomes] |
rs72640809 | 0.82[EUR][1000 genomes] |
rs72640869 | 0.81[EUR][1000 genomes] |
rs72640870 | 0.85[EUR][1000 genomes] |
rs72640871 | 0.85[EUR][1000 genomes] |
rs72640872 | 0.85[EUR][1000 genomes] |
rs73437905 | 0.87[EUR][1000 genomes] |
rs73437936 | 0.87[EUR][1000 genomes] |
rs73437939 | 0.87[EUR][1000 genomes] |
rs73437947 | 0.85[EUR][1000 genomes] |
rs73437955 | 0.87[EUR][1000 genomes] |
rs73437958 | 0.87[EUR][1000 genomes] |
rs73437965 | 0.87[EUR][1000 genomes] |
rs73437973 | 0.87[EUR][1000 genomes] |
rs73437989 | 0.85[EUR][1000 genomes] |
rs73438001 | 0.85[EUR][1000 genomes] |
rs73455517 | 0.80[EUR][1000 genomes] |
rs73455527 | 0.80[EUR][1000 genomes] |
rs73455539 | 0.85[EUR][1000 genomes] |
rs73455545 | 0.87[EUR][1000 genomes] |
rs73455552 | 0.87[EUR][1000 genomes] |
rs73455553 | 0.87[EUR][1000 genomes] |
rs7480202 | 0.80[EUR][1000 genomes] |
rs7926684 | 0.87[EUR][1000 genomes] |
rs7927358 | 0.87[EUR][1000 genomes] |
rs7929473 | 0.85[EUR][1000 genomes] |
rs7937683 | 0.85[EUR][1000 genomes] |
rs7944879 | 0.87[EUR][1000 genomes] |
rs7946993 | 0.87[EUR][1000 genomes] |
rs867801 | 0.85[EUR][1000 genomes] |
rs867804 | 0.85[EUR][1000 genomes] |
rs868613 | 0.87[EUR][1000 genomes] |
rs869206 | 0.85[EUR][1000 genomes] |
rs885374 | 0.87[EUR][1000 genomes] |
rs969611 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv467791 | chr11:36108497-36999385 | Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
2 | nsv554003 | chr11:36108497-36999385 | ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
3 | nsv832123 | chr11:36582872-36757443 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
4 | nsv467792 | chr11:36624187-36898373 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv554005 | chr11:36624187-36898373 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv467793 | chr11:36632515-37171833 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv554006 | chr11:36632515-37171833 | Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv1047073 | chr11:36711638-36812910 | Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
9 | nsv1041508 | chr11:36711638-36815367 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv1043391 | chr11:36711638-36817144 | Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
11 | nsv554007 | chr11:36711834-36825618 | Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
12 | esv11137 | chr11:36730247-36788022 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
13 | esv2761663 | chr11:36730335-36786817 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:36746800-36759600 | Weak transcription | Thymus | Thymus |