Variant report
Variant | rs2169895 |
---|---|
Chromosome Location | chr1:150027486-150027487 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000178096 | Chromatin interaction |
ENSG00000184270 | Chromatin interaction |
ENSG00000136631 | Chromatin interaction |
ENSG00000184260 | Chromatin interaction |
ENSG00000184678 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10494264 | 0.88[EUR][1000 genomes] |
rs10749674 | 0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs10888568 | 0.93[EUR][1000 genomes] |
rs10888569 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs10888572 | 0.86[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs11205316 | 0.86[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs11205317 | 0.92[EUR][1000 genomes] |
rs11205319 | 0.92[EUR][1000 genomes] |
rs11205321 | 0.94[EUR][1000 genomes] |
rs11205326 | 0.96[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs11205329 | 0.83[EUR][1000 genomes] |
rs11205331 | 0.91[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs11205333 | 0.88[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs11577346 | 0.86[EUR][1000 genomes] |
rs11583720 | 0.90[EUR][1000 genomes] |
rs11584091 | 0.86[EUR][1000 genomes] |
rs11584354 | 0.91[EUR][1000 genomes] |
rs11585955 | 0.90[EUR][1000 genomes] |
rs11587963 | 0.86[EUR][1000 genomes] |
rs11589585 | 0.92[EUR][1000 genomes] |
rs11589922 | 0.82[EUR][1000 genomes] |
rs11591200 | 0.82[EUR][1000 genomes] |
rs12058090 | 0.92[EUR][1000 genomes] |
rs12058502 | 0.91[EUR][1000 genomes] |
rs12060027 | 0.93[EUR][1000 genomes] |
rs12060211 | 0.92[EUR][1000 genomes] |
rs12061167 | 0.92[EUR][1000 genomes] |
rs12061196 | 0.92[EUR][1000 genomes] |
rs12061565 | 0.91[EUR][1000 genomes] |
rs12061856 | 0.91[EUR][1000 genomes] |
rs12062861 | 0.91[EUR][1000 genomes] |
rs12063059 | 0.92[EUR][1000 genomes] |
rs12063281 | 0.91[EUR][1000 genomes] |
rs12063329 | 0.91[EUR][1000 genomes] |
rs12064532 | 0.88[EUR][1000 genomes] |
rs12065681 | 0.92[EUR][1000 genomes] |
rs12066132 | 0.92[EUR][1000 genomes] |
rs12066293 | 0.92[EUR][1000 genomes] |
rs12067422 | 0.92[EUR][1000 genomes] |
rs12073359 | 0.91[EUR][1000 genomes] |
rs12074281 | 0.94[EUR][1000 genomes] |
rs12093499 | 0.91[EUR][1000 genomes] |
rs12098106 | 0.91[EUR][1000 genomes] |
rs12139248 | 0.82[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs1339494 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1339495 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1382573 | 0.82[EUR][1000 genomes] |
rs1545762 | 0.88[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs1824847 | 0.90[AFR][1000 genomes] |
rs1824848 | 0.80[EUR][1000 genomes] |
rs1824849 | 0.82[EUR][1000 genomes] |
rs1824850 | 0.82[EUR][1000 genomes] |
rs1964542 | 1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1975957 | 0.91[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs2027349 | 0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2039800 | 0.88[EUR][1000 genomes] |
rs2318763 | 0.86[EUR][1000 genomes] |
rs2319280 | 0.91[EUR][1000 genomes] |
rs28366567 | 0.90[EUR][1000 genomes] |
rs28443768 | 0.91[EUR][1000 genomes] |
rs28560140 | 0.92[EUR][1000 genomes] |
rs28660389 | 0.93[EUR][1000 genomes] |
rs28753817 | 0.92[EUR][1000 genomes] |
rs3208509 | 0.82[EUR][1000 genomes] |
rs3850838 | 0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs3925724 | 0.88[EUR][1000 genomes] |
rs4058847 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs4926388 | 1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs4926391 | 0.80[EUR][1000 genomes] |
rs4926406 | 0.83[EUR][1000 genomes] |
rs4926407 | 0.94[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4926408 | 0.90[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs4926409 | 0.90[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs55633125 | 0.92[EUR][1000 genomes] |
rs55647342 | 0.95[EUR][1000 genomes] |
rs55802315 | 0.81[EUR][1000 genomes] |
rs55840680 | 0.86[EUR][1000 genomes] |
rs55840906 | 0.91[EUR][1000 genomes] |
rs55909733 | 0.86[EUR][1000 genomes] |
rs55918911 | 0.93[EUR][1000 genomes] |
rs56125600 | 0.93[EUR][1000 genomes] |
rs56188926 | 0.89[EUR][1000 genomes] |
rs56212907 | 0.89[EUR][1000 genomes] |
rs56349882 | 0.82[EUR][1000 genomes] |
rs56369603 | 0.86[EUR][1000 genomes] |
rs57926929 | 0.87[EUR][1000 genomes] |
rs58426216 | 0.84[EUR][1000 genomes] |
rs59607464 | 0.82[EUR][1000 genomes] |
rs6657062 | 0.88[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs6666959 | 0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs6687454 | 0.91[EUR][1000 genomes] |
rs6694729 | 0.96[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs72692857 | 0.91[EUR][1000 genomes] |
rs72692861 | 0.91[EUR][1000 genomes] |
rs72692862 | 0.91[EUR][1000 genomes] |
rs72692865 | 0.92[EUR][1000 genomes] |
rs72692866 | 0.92[EUR][1000 genomes] |
rs72692869 | 0.92[EUR][1000 genomes] |
rs72692886 | 0.91[EUR][1000 genomes] |
rs72692893 | 0.89[EUR][1000 genomes] |
rs72692895 | 0.90[EUR][1000 genomes] |
rs72692896 | 0.90[EUR][1000 genomes] |
rs72692897 | 0.90[EUR][1000 genomes] |
rs72692898 | 0.89[EUR][1000 genomes] |
rs72692899 | 0.89[EUR][1000 genomes] |
rs72692900 | 0.89[EUR][1000 genomes] |
rs72692901 | 0.90[EUR][1000 genomes] |
rs72694905 | 0.87[EUR][1000 genomes] |
rs72694906 | 0.89[EUR][1000 genomes] |
rs72694908 | 0.89[EUR][1000 genomes] |
rs72694914 | 0.88[EUR][1000 genomes] |
rs72694915 | 0.88[EUR][1000 genomes] |
rs72694917 | 0.89[EUR][1000 genomes] |
rs72694918 | 0.89[EUR][1000 genomes] |
rs72694919 | 0.89[EUR][1000 genomes] |
rs72694923 | 0.88[EUR][1000 genomes] |
rs72694926 | 0.86[EUR][1000 genomes] |
rs72694927 | 0.87[EUR][1000 genomes] |
rs72694928 | 0.86[EUR][1000 genomes] |
rs72694933 | 0.86[EUR][1000 genomes] |
rs72694936 | 0.86[EUR][1000 genomes] |
rs72694942 | 0.86[EUR][1000 genomes] |
rs72694943 | 0.87[EUR][1000 genomes] |
rs72694944 | 0.86[EUR][1000 genomes] |
rs72694945 | 0.86[EUR][1000 genomes] |
rs72694946 | 0.86[EUR][1000 genomes] |
rs72694950 | 0.86[EUR][1000 genomes] |
rs72694951 | 0.86[EUR][1000 genomes] |
rs72694953 | 0.86[EUR][1000 genomes] |
rs72694954 | 0.85[EUR][1000 genomes] |
rs72694956 | 0.82[EUR][1000 genomes] |
rs72694957 | 0.82[EUR][1000 genomes] |
rs72694959 | 0.81[EUR][1000 genomes] |
rs7519918 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7520930 | 0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7530922 | 0.92[EUR][1000 genomes] |
rs7540847 | 0.94[EUR][1000 genomes] |
rs7550323 | 0.94[EUR][1000 genomes] |
rs7550350 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7553622 | 0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7554367 | 0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7555080 | 0.96[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs9662055 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831537 | chr1:149833357-150064655 | Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 431 gene(s) | inside rSNPs | diseases |
2 | nsv529719 | chr1:150006344-150311095 | Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 100 gene(s) | inside rSNPs | diseases |
3 | nsv947321 | chr1:150007387-150030042 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:149996600-150037000 | Weak transcription | Left Ventricle | heart |
2 | chr1:150017600-150037600 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
3 | chr1:150018000-150031600 | Weak transcription | Stomach Smooth Muscle | stomach |
4 | chr1:150018000-150033400 | Weak transcription | Fetal Stomach | stomach |
5 | chr1:150018200-150038600 | Weak transcription | Fetal Muscle Trunk | muscle |
6 | chr1:150022800-150032400 | Weak transcription | Fetal Intestine Small | intestine |
7 | chr1:150022800-150037200 | Weak transcription | Brain Dorsolateral Prefrontal Cortex | brain |
8 | chr1:150022800-150038600 | Weak transcription | Brain Inferior Temporal Lobe | brain |
9 | chr1:150023000-150028600 | Weak transcription | Primary B cells from cord blood | blood |
10 | chr1:150023000-150033600 | Weak transcription | Colon Smooth Muscle | Colon |
11 | chr1:150026400-150033600 | Weak transcription | NHDF-Ad | bronchial |
12 | chr1:150026400-150033800 | Weak transcription | Right Atrium | heart |
13 | chr1:150026600-150029600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
14 | chr1:150027000-150028200 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
15 | chr1:150027200-150027800 | Weak transcription | Primary monocytes fromperipheralblood | blood |