Variant report
Variant | rs7542784 |
---|---|
Chromosome Location | chr1:161345367-161345368 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000158859 | Chromatin interaction |
ENSG00000158864 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10157158 | 0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10157457 | 0.88[ASN][1000 genomes] |
rs10157990 | 0.87[ASN][1000 genomes] |
rs10157991 | 0.86[ASN][1000 genomes] |
rs10158388 | 0.97[ASN][1000 genomes] |
rs10159083 | 0.94[ASN][1000 genomes] |
rs10494350 | 0.97[ASN][1000 genomes] |
rs10494351 | 0.97[ASN][1000 genomes] |
rs10494352 | 0.97[ASN][1000 genomes] |
rs10494353 | 0.97[ASN][1000 genomes] |
rs10494354 | 0.97[ASN][1000 genomes] |
rs10494355 | 0.88[ASN][1000 genomes] |
rs1133805 | 0.97[ASN][1000 genomes] |
rs1133806 | 0.97[ASN][1000 genomes] |
rs11582439 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11588994 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12239492 | 0.96[ASN][1000 genomes] |
rs12239719 | 0.97[ASN][1000 genomes] |
rs12385723 | 0.93[ASN][1000 genomes] |
rs12385733 | 0.97[ASN][1000 genomes] |
rs12725465 | 0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12730813 | 0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12737323 | 0.82[ASN][1000 genomes] |
rs12738660 | 0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12745476 | 0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12757174 | 0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13374037 | 0.97[ASN][1000 genomes] |
rs13375385 | 0.95[ASN][1000 genomes] |
rs13375937 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13376158 | 0.95[ASN][1000 genomes] |
rs16832809 | 0.88[ASN][1000 genomes] |
rs16832811 | 0.88[ASN][1000 genomes] |
rs16832813 | 0.88[ASN][1000 genomes] |
rs16832817 | 0.90[ASN][1000 genomes] |
rs16832820 | 0.90[ASN][1000 genomes] |
rs16832823 | 0.90[ASN][1000 genomes] |
rs16832824 | 0.91[ASN][1000 genomes] |
rs16832826 | 0.94[ASN][1000 genomes] |
rs16832835 | 0.97[ASN][1000 genomes] |
rs16832842 | 0.97[ASN][1000 genomes] |
rs16832846 | 0.97[ASN][1000 genomes] |
rs16832851 | 0.97[ASN][1000 genomes] |
rs16832854 | 0.97[ASN][1000 genomes] |
rs16832869 | 0.97[ASN][1000 genomes] |
rs16832871 | 0.97[ASN][1000 genomes] |
rs16832874 | 0.97[ASN][1000 genomes] |
rs16832883 | 0.96[ASN][1000 genomes] |
rs16832884 | 0.97[ASN][1000 genomes] |
rs16832887 | 0.97[ASN][1000 genomes] |
rs16832892 | 0.96[ASN][1000 genomes] |
rs16832894 | 0.97[ASN][1000 genomes] |
rs16832897 | 0.97[ASN][1000 genomes] |
rs16832900 | 0.97[ASN][1000 genomes] |
rs16832902 | 0.97[ASN][1000 genomes] |
rs16832908 | 0.97[ASN][1000 genomes] |
rs16832922 | 0.97[ASN][1000 genomes] |
rs16832948 | 0.88[ASN][1000 genomes] |
rs3087596 | 0.97[ASN][1000 genomes] |
rs34538569 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs34872203 | 0.95[ASN][1000 genomes] |
rs35006684 | 0.97[ASN][1000 genomes] |
rs35130144 | 0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs35215727 | 0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs35680024 | 0.94[ASN][1000 genomes] |
rs3934593 | 0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3935401 | 0.97[ASN][1000 genomes] |
rs4077289 | 0.97[ASN][1000 genomes] |
rs4077290 | 0.97[ASN][1000 genomes] |
rs4077631 | 0.96[ASN][1000 genomes] |
rs41270861 | 0.97[ASN][1000 genomes] |
rs4255402 | 0.94[ASN][1000 genomes] |
rs4291521 | 0.96[ASN][1000 genomes] |
rs4319356 | 0.97[ASN][1000 genomes] |
rs4360541 | 0.95[ASN][1000 genomes] |
rs4400628 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4463689 | 0.97[ASN][1000 genomes] |
rs4469725 | 0.95[ASN][1000 genomes] |
rs4474277 | 0.93[ASN][1000 genomes] |
rs4477296 | 0.95[ASN][1000 genomes] |
rs4481873 | 0.97[ASN][1000 genomes] |
rs4525064 | 0.97[ASN][1000 genomes] |
rs4534403 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4534404 | 0.97[ASN][1000 genomes] |
rs4534405 | 0.97[ASN][1000 genomes] |
rs4585997 | 0.97[ASN][1000 genomes] |
rs4600063 | 0.97[ASN][1000 genomes] |
rs4622080 | 0.94[ASN][1000 genomes] |
rs4631719 | 0.95[ASN][1000 genomes] |
rs4634926 | 0.97[ASN][1000 genomes] |
rs4634927 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55674249 | 0.96[ASN][1000 genomes] |
rs55682614 | 0.94[ASN][1000 genomes] |
rs55690323 | 0.87[ASN][1000 genomes] |
rs55698724 | 0.96[ASN][1000 genomes] |
rs55729989 | 0.97[ASN][1000 genomes] |
rs55747162 | 0.90[ASN][1000 genomes] |
rs55775286 | 0.86[ASN][1000 genomes] |
rs55783815 | 0.97[ASN][1000 genomes] |
rs55807618 | 0.97[ASN][1000 genomes] |
rs55809622 | 0.97[ASN][1000 genomes] |
rs55839314 | 0.90[ASN][1000 genomes] |
rs55898518 | 0.91[ASN][1000 genomes] |
rs55929617 | 0.97[ASN][1000 genomes] |
rs55955603 | 0.80[ASN][1000 genomes] |
rs55961103 | 0.94[ASN][1000 genomes] |
rs55962831 | 0.95[ASN][1000 genomes] |
rs55981028 | 0.90[ASN][1000 genomes] |
rs55996762 | 0.96[ASN][1000 genomes] |
rs56007456 | 0.97[ASN][1000 genomes] |
rs56028608 | 0.96[ASN][1000 genomes] |
rs56062031 | 0.96[ASN][1000 genomes] |
rs56071922 | 0.93[ASN][1000 genomes] |
rs56122953 | 0.96[ASN][1000 genomes] |
rs56169917 | 0.96[ASN][1000 genomes] |
rs56269923 | 0.93[ASN][1000 genomes] |
rs56280055 | 0.88[ASN][1000 genomes] |
rs56290916 | 0.97[ASN][1000 genomes] |
rs56291729 | 0.88[ASN][1000 genomes] |
rs56355322 | 0.90[ASN][1000 genomes] |
rs56358807 | 0.86[ASN][1000 genomes] |
rs56406825 | 0.97[ASN][1000 genomes] |
rs56411570 | 0.94[ASN][1000 genomes] |
rs56868836 | 0.97[ASN][1000 genomes] |
rs57007882 | 0.97[ASN][1000 genomes] |
rs57154376 | 0.96[ASN][1000 genomes] |
rs57270150 | 0.97[ASN][1000 genomes] |
rs57306652 | 0.97[ASN][1000 genomes] |
rs57421557 | 0.97[ASN][1000 genomes] |
rs57473118 | 0.97[ASN][1000 genomes] |
rs57474688 | 0.96[ASN][1000 genomes] |
rs57835711 | 0.97[ASN][1000 genomes] |
rs57841279 | 0.97[ASN][1000 genomes] |
rs57858140 | 0.97[ASN][1000 genomes] |
rs58055613 | 0.92[ASN][1000 genomes] |
rs58138146 | 0.97[ASN][1000 genomes] |
rs58418155 | 0.96[ASN][1000 genomes] |
rs58758353 | 0.91[ASN][1000 genomes] |
rs58840032 | 0.88[ASN][1000 genomes] |
rs58842513 | 0.97[ASN][1000 genomes] |
rs58874147 | 0.97[ASN][1000 genomes] |
rs59037769 | 0.95[ASN][1000 genomes] |
rs59191996 | 0.97[ASN][1000 genomes] |
rs59340690 | 0.97[ASN][1000 genomes] |
rs59544428 | 0.97[ASN][1000 genomes] |
rs59559479 | 0.97[ASN][1000 genomes] |
rs59690240 | 0.90[ASN][1000 genomes] |
rs59747425 | 0.97[ASN][1000 genomes] |
rs59774375 | 0.97[ASN][1000 genomes] |
rs59840298 | 0.97[ASN][1000 genomes] |
rs60078979 | 0.93[ASN][1000 genomes] |
rs60179510 | 0.97[ASN][1000 genomes] |
rs60261157 | 0.89[ASN][1000 genomes] |
rs60309040 | 0.93[ASN][1000 genomes] |
rs60345130 | 0.93[ASN][1000 genomes] |
rs60382588 | 0.97[ASN][1000 genomes] |
rs60405593 | 0.96[ASN][1000 genomes] |
rs60435895 | 0.93[ASN][1000 genomes] |
rs60792683 | 0.94[ASN][1000 genomes] |
rs60799370 | 0.93[ASN][1000 genomes] |
rs60882053 | 0.96[ASN][1000 genomes] |
rs61181161 | 0.96[ASN][1000 genomes] |
rs61219424 | 0.96[ASN][1000 genomes] |
rs61299084 | 0.95[ASN][1000 genomes] |
rs61304797 | 0.86[ASN][1000 genomes] |
rs61308286 | 0.97[ASN][1000 genomes] |
rs61410886 | 0.88[ASN][1000 genomes] |
rs61447446 | 0.97[ASN][1000 genomes] |
rs61461118 | 0.97[ASN][1000 genomes] |
rs61576374 | 0.97[ASN][1000 genomes] |
rs61608953 | 0.88[ASN][1000 genomes] |
rs61618989 | 0.94[ASN][1000 genomes] |
rs61653684 | 0.97[ASN][1000 genomes] |
rs6668174 | 0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6670076 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6675552 | 0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6688180 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6693070 | 0.81[EUR][1000 genomes] |
rs7412460 | 0.95[ASN][1000 genomes] |
rs74124931 | 0.96[ASN][1000 genomes] |
rs74124933 | 0.88[ASN][1000 genomes] |
rs74127622 | 0.94[ASN][1000 genomes] |
rs74127629 | 0.96[ASN][1000 genomes] |
rs74127630 | 0.96[ASN][1000 genomes] |
rs74127635 | 0.96[ASN][1000 genomes] |
rs74127636 | 0.96[ASN][1000 genomes] |
rs74127638 | 0.97[ASN][1000 genomes] |
rs74127639 | 0.97[ASN][1000 genomes] |
rs74127641 | 0.97[ASN][1000 genomes] |
rs74127657 | 0.97[ASN][1000 genomes] |
rs74127658 | 0.97[ASN][1000 genomes] |
rs9330294 | 0.97[ASN][1000 genomes] |
rs9970904 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv432986 | chr1:161221133-161673682 | Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
2 | nsv1010776 | chr1:161282384-161409218 | Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 46 gene(s) | inside rSNPs | diseases |
3 | nsv432998 | chr1:161335902-161673682 | Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 62 gene(s) | inside rSNPs | diseases |
4 | nsv872493 | chr1:161339060-161413794 | Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 42 gene(s) | inside rSNPs | diseases |
5 | nsv433009 | chr1:161343927-161639328 | Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 58 gene(s) | inside rSNPs | diseases |
6 | nsv1005812 | chr1:161343951-161548101 | Weak transcription Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 55 gene(s) | inside rSNPs | diseases |
7 | nsv535182 | chr1:161343951-161548101 | Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 55 gene(s) | inside rSNPs | diseases |
8 | esv2756866 | chr1:161344255-161681552 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 62 gene(s) | inside rSNPs | diseases |
9 | esv2758972 | chr1:161344255-161681552 | Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 62 gene(s) | inside rSNPs | diseases |
10 | nsv825154 | chr1:161344705-161346698 | Enhancers Weak transcription | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:161321800-161348800 | Weak transcription | Gastric | stomach |
2 | chr1:161327400-161352600 | Weak transcription | Lung | lung |
3 | chr1:161328400-161359000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr1:161328600-161359000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
5 | chr1:161335000-161356000 | Weak transcription | K562 | blood |
6 | chr1:161336400-161348800 | Weak transcription | Placenta | Placenta |
7 | chr1:161336600-161351600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
8 | chr1:161336600-161352200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
9 | chr1:161336600-161352200 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
10 | chr1:161336800-161348600 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
11 | chr1:161336800-161348800 | Weak transcription | Fetal Muscle Leg | muscle |
12 | chr1:161336800-161348800 | Weak transcription | Fetal Thymus | thymus |
13 | chr1:161336800-161351600 | Weak transcription | NHEK | skin |
14 | chr1:161337800-161348800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
15 | chr1:161337800-161356200 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
16 | chr1:161338000-161346000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
17 | chr1:161338000-161351600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
18 | chr1:161338000-161356000 | Weak transcription | GM12878-XiMat | blood |
19 | chr1:161338200-161348600 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
20 | chr1:161338600-161346800 | Weak transcription | HepG2 | liver |
21 | chr1:161344400-161348800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
22 | chr1:161344600-161348800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |