Variant report
Variant | rs583989 |
---|---|
Chromosome Location | chr11:100768003-100768004 |
allele | A/G |
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] |
---|---|
rs10791434 | 0.89[AFR][1000 genomes] |
rs10791435 | 0.89[AFR][1000 genomes] |
rs10791437 | 0.89[AFR][1000 genomes] |
rs10791438 | 0.89[AFR][1000 genomes] |
rs10895031 | 0.89[AFR][1000 genomes] |
rs11224535 | 0.89[AFR][1000 genomes] |
rs1217180 | 0.94[EUR][1000 genomes] |
rs1941370 | 0.81[EUR][1000 genomes] |
rs1941371 | 0.81[EUR][1000 genomes] |
rs1941372 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs2155442 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs2155793 | 0.81[EUR][1000 genomes] |
rs2510624 | 0.89[AFR][1000 genomes] |
rs2510625 | 0.87[AFR][1000 genomes] |
rs2510626 | 0.87[AFR][1000 genomes] |
rs3017866 | 0.89[AFR][1000 genomes] |
rs471180 | 0.81[EUR][1000 genomes] |
rs474651 | 0.85[AFR][1000 genomes] |
rs4753987 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs475432 | 0.81[AFR][1000 genomes] |
rs477567 | 0.89[AFR][1000 genomes] |
rs480080 | 0.89[AFR][1000 genomes] |
rs480145 | 0.81[AFR][1000 genomes] |
rs481991 | 0.89[AFR][1000 genomes] |
rs483789 | 0.89[AFR][1000 genomes] |
rs493079 | 0.89[AFR][1000 genomes] |
rs494451 | 0.87[AFR][1000 genomes] |
rs494907 | 0.84[AFR][1000 genomes] |
rs497234 | 0.81[AFR][1000 genomes] |
rs501797 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs501831 | 0.81[AFR][1000 genomes] |
rs503455 | 0.89[AFR][1000 genomes] |
rs505405 | 0.84[AFR][1000 genomes] |
rs506242 | 0.89[AFR][1000 genomes] |
rs508850 | 0.89[AFR][1000 genomes] |
rs508950 | 0.89[AFR][1000 genomes] |
rs509013 | 0.89[AFR][1000 genomes] |
rs509166 | 0.89[AFR][1000 genomes] |
rs509676 | 0.89[AFR][1000 genomes] |
rs512176 | 0.82[AFR][1000 genomes] |
rs513057 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs514101 | 0.89[AFR][1000 genomes] |
rs514403 | 0.89[AFR][1000 genomes] |
rs518675 | 0.89[AFR][1000 genomes] |
rs519235 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs519594 | 0.89[AFR][1000 genomes] |
rs520403 | 0.81[EUR][1000 genomes] |
rs520539 | 0.89[AFR][1000 genomes] |
rs521216 | 0.83[AFR][1000 genomes] |
rs522337 | 0.89[AFR][1000 genomes] |
rs524416 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs525129 | 0.89[AFR][1000 genomes] |
rs529194 | 0.81[EUR][1000 genomes] |
rs532783 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs534623 | 0.89[AFR][1000 genomes] |
rs535518 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs536270 | 0.87[AFR][1000 genomes] |
rs538158 | 0.89[AFR][1000 genomes] |
rs539204 | 0.89[AFR][1000 genomes] |
rs540000 | 0.85[AFR][1000 genomes] |
rs540961 | 0.89[AFR][1000 genomes] |
rs541056 | 0.89[AFR][1000 genomes] |
rs544257 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs544388 | 0.89[AFR][1000 genomes] |
rs546052 | 0.81[EUR][1000 genomes] |
rs546059 | 0.94[EUR][1000 genomes] |
rs547105 | 0.81[EUR][1000 genomes] |
rs549510 | 0.81[AFR][1000 genomes] |
rs551502 | 0.89[AFR][1000 genomes] |
rs555825 | 0.81[AFR][1000 genomes] |
rs560235 | 0.81[EUR][1000 genomes] |
rs562891 | 0.89[AFR][1000 genomes] |
rs566608 | 0.85[AFR][1000 genomes] |
rs571904 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs572838 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs575448 | 0.89[AFR][1000 genomes] |
rs577170 | 0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs578102 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs580773 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs584029 | 0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs594200 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs595761 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs601016 | 0.81[AFR][1000 genomes] |
rs607889 | 0.91[EUR][1000 genomes] |
rs614393 | 0.88[EUR][1000 genomes] |
rs614761 | 0.88[EUR][1000 genomes] |
rs616164 | 0.89[AFR][1000 genomes] |
rs617898 | 0.89[AFR][1000 genomes] |
rs618017 | 0.81[AFR][1000 genomes] |
rs618155 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs618907 | 0.89[AFR][1000 genomes] |
rs619066 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs620790 | 0.89[AFR][1000 genomes] |
rs621172 | 0.85[AFR][1000 genomes] |
rs629442 | 0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs629677 | 0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs632725 | 0.89[AFR][1000 genomes] |
rs633967 | 0.89[AFR][1000 genomes] |
rs636528 | 0.88[EUR][1000 genomes] |
rs637508 | 0.81[EUR][1000 genomes] |
rs638004 | 0.81[EUR][1000 genomes] |
rs641341 | 0.82[AFR][1000 genomes] |
rs641948 | 0.91[EUR][1000 genomes] |
rs649369 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs649394 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs650269 | 0.81[EUR][1000 genomes] |
rs652017 | 0.87[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs652559 | 0.87[AFR][1000 genomes] |
rs662173 | 0.89[AFR][1000 genomes] |
rs663622 | 0.87[AFR][1000 genomes] |
rs673183 | 0.82[AFR][1000 genomes] |
rs676976 | 0.89[AFR][1000 genomes] |
rs678351 | 0.87[AFR][1000 genomes] |
rs678775 | 0.89[AFR][1000 genomes] |
rs688664 | 0.91[EUR][1000 genomes] |
rs693760 | 0.89[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs694556 | 0.85[AFR][1000 genomes] |
rs7929787 | 0.85[AFR][1000 genomes] |
rs7933457 | 0.89[AFR][1000 genomes] |
rs7938783 | 0.82[AFR][1000 genomes] |
rs7952007 | 0.83[AFR][1000 genomes] |
rs7952634 | 0.85[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1048356 | chr11:100713096-101058995 | Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | nsv541154 | chr11:100713096-101058995 | Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:100758400-100798400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr11:100758600-100773400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr11:100758600-100795200 | Weak transcription | Fetal Muscle Trunk | muscle |
4 | chr11:100758800-100789400 | Weak transcription | Fetal Muscle Leg | muscle |
5 | chr11:100758800-100791200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
6 | chr11:100761000-100773400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
7 | chr11:100761600-100777400 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
8 | chr11:100761600-100788800 | Weak transcription | Fetal Heart | heart |
9 | chr11:100761800-100773400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
10 | chr11:100762800-100779000 | Weak transcription | NH-A | brain |