Variant report
Variant | rs10489714 |
---|---|
Chromosome Location | chr1:185744111-185744112 |
allele | A/G |
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 |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10047250 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10449224 | 1.00[ASN][1000 genomes] |
rs10465497 | 1.00[ASN][1000 genomes] |
rs10465500 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10489713 | 1.00[CHB][hapmap] |
rs10489715 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10489716 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10489717 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10911781 | 1.00[JPT][hapmap] |
rs10911785 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10911789 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs10911790 | 1.00[ASN][1000 genomes] |
rs1124755 | 1.00[EUR][1000 genomes] |
rs1124756 | 1.00[CHB][hapmap] |
rs11800990 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs11807146 | 1.00[JPT][hapmap] |
rs12078444 | 1.00[JPT][hapmap] |
rs12095309 | 1.00[ASN][1000 genomes] |
rs12164583 | 1.00[EUR][1000 genomes] |
rs12239929 | 1.00[JPT][hapmap] |
rs1321670 | 1.00[JPT][hapmap] |
rs1321671 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1321672 | 1.00[CHB][hapmap] |
rs1321673 | 1.00[CHB][hapmap] |
rs13374445 | 1.00[JPT][hapmap] |
rs1407426 | 1.00[JPT][hapmap] |
rs1407428 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs1407429 | 1.00[JPT][hapmap] |
rs1555494 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs16824426 | 1.00[CHB][hapmap] |
rs16824427 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs16824428 | 1.00[CHB][hapmap] |
rs16824451 | 1.00[CHB][hapmap] |
rs16824455 | 1.00[CHB][hapmap] |
rs16824458 | 1.00[CHB][hapmap] |
rs16824465 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16824488 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs16824497 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs16824524 | 1.00[CHB][hapmap] |
rs16824576 | 1.00[JPT][hapmap] |
rs17505819 | 1.00[JPT][hapmap] |
rs1825398 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs1830622 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs1830623 | 1.00[ASN][1000 genomes] |
rs1853247 | 1.00[ASN][1000 genomes] |
rs2129125 | 1.00[JPT][hapmap] |
rs2170858 | 1.00[ASN][1000 genomes] |
rs2200266 | 1.00[CHB][hapmap] |
rs28666501 | 1.00[EUR][1000 genomes] |
rs28754345 | 1.00[EUR][1000 genomes] |
rs55683049 | 1.00[EUR][1000 genomes] |
rs55887884 | 1.00[ASN][1000 genomes] |
rs55954704 | 1.00[EUR][1000 genomes] |
rs56331179 | 1.00[ASN][1000 genomes] |
rs57107751 | 1.00[ASN][1000 genomes] |
rs57123319 | 1.00[EUR][1000 genomes] |
rs57162167 | 1.00[ASN][1000 genomes] |
rs57215320 | 1.00[ASN][1000 genomes] |
rs57246058 | 1.00[ASN][1000 genomes] |
rs57257586 | 1.00[ASN][1000 genomes] |
rs57646829 | 1.00[ASN][1000 genomes] |
rs57775662 | 1.00[EUR][1000 genomes] |
rs57782754 | 1.00[ASN][1000 genomes] |
rs58131117 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58135888 | 1.00[EUR][1000 genomes] |
rs58140638 | 1.00[EUR][1000 genomes] |
rs58159343 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58291464 | 1.00[ASN][1000 genomes] |
rs58433773 | 1.00[ASN][1000 genomes] |
rs58437418 | 1.00[ASN][1000 genomes] |
rs58449767 | 1.00[EUR][1000 genomes] |
rs58597777 | 1.00[EUR][1000 genomes] |
rs58609803 | 1.00[EUR][1000 genomes] |
rs58610258 | 1.00[ASN][1000 genomes] |
rs59175860 | 1.00[ASN][1000 genomes] |
rs59312002 | 1.00[ASN][1000 genomes] |
rs59967839 | 1.00[ASN][1000 genomes] |
rs60134058 | 1.00[EUR][1000 genomes] |
rs60308365 | 1.00[ASN][1000 genomes] |
rs60458315 | 1.00[ASN][1000 genomes] |
rs60735946 | 1.00[ASN][1000 genomes] |
rs61088604 | 1.00[EUR][1000 genomes] |
rs61103306 | 1.00[EUR][1000 genomes] |
rs61261990 | 1.00[ASN][1000 genomes] |
rs61315386 | 1.00[EUR][1000 genomes] |
rs61679640 | 1.00[ASN][1000 genomes] |
rs61689983 | 1.00[ASN][1000 genomes] |
rs6425001 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6425004 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6425005 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6425006 | 1.00[EUR][1000 genomes] |
rs6657554 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6657683 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6660510 | 1.00[JPT][hapmap] |
rs6662653 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6667316 | 1.00[JPT][hapmap] |
rs6671094 | 1.00[ASN][1000 genomes] |
rs6675465 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6675691 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6676522 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6676629 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6676765 | 1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6676937 | 1.00[CHB][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6677167 | 1.00[CHB][hapmap] |
rs6677183 | 1.00[ASN][1000 genomes] |
rs6679816 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6683809 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6685093 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6686790 | 1.00[EUR][1000 genomes] |
rs6686816 | 1.00[ASN][1000 genomes] |
rs6688298 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6688369 | 1.00[ASN][1000 genomes] |
rs6689359 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6690475 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6690559 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6690714 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6696804 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6698721 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6700856 | 1.00[ASN][1000 genomes] |
rs726777 | 1.00[JPT][hapmap] |
rs72703022 | 1.00[ASN][1000 genomes] |
rs72703023 | 1.00[ASN][1000 genomes] |
rs72718868 | 1.00[ASN][1000 genomes] |
rs72718870 | 1.00[ASN][1000 genomes] |
rs73054403 | 1.00[ASN][1000 genomes] |
rs73054407 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73058398 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73058399 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73058401 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73060462 | 1.00[EUR][1000 genomes] |
rs73060467 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73060474 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73062155 | 1.00[ASN][1000 genomes] |
rs73062157 | 1.00[ASN][1000 genomes] |
rs73062161 | 1.00[ASN][1000 genomes] |
rs73062164 | 1.00[ASN][1000 genomes] |
rs73062166 | 1.00[ASN][1000 genomes] |
rs73062512 | 1.00[ASN][1000 genomes] |
rs73062516 | 1.00[ASN][1000 genomes] |
rs73070519 | 1.00[ASN][1000 genomes] |
rs73070522 | 1.00[ASN][1000 genomes] |
rs73070547 | 1.00[ASN][1000 genomes] |
rs73070548 | 1.00[ASN][1000 genomes] |
rs73070567 | 1.00[ASN][1000 genomes] |
rs73070598 | 1.00[ASN][1000 genomes] |
rs73070601 | 1.00[EUR][1000 genomes] |
rs73072006 | 1.00[EUR][1000 genomes] |
rs73072009 | 1.00[EUR][1000 genomes] |
rs73072046 | 1.00[EUR][1000 genomes] |
rs73072051 | 1.00[EUR][1000 genomes] |
rs73072052 | 1.00[EUR][1000 genomes] |
rs73072056 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73072059 | 1.00[EUR][1000 genomes] |
rs73072077 | 1.00[ASN][1000 genomes] |
rs74133680 | 1.00[EUR][1000 genomes] |
rs74135350 | 1.00[ASN][1000 genomes] |
rs74135351 | 1.00[ASN][1000 genomes] |
rs7517811 | 1.00[ASN][1000 genomes] |
rs7519398 | 1.00[ASN][1000 genomes] |
rs7521401 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7532062 | 1.00[ASN][1000 genomes] |
rs7532431 | 1.00[ASN][1000 genomes] |
rs7540727 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs7540773 | 1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7541361 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7544162 | 1.00[ASN][1000 genomes] |
rs7544533 | 1.00[JPT][hapmap] |
rs7544808 | 1.00[ASN][1000 genomes] |
rs7546152 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7547368 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7555536 | 1.00[ASN][1000 genomes] |
rs959689 | 1.00[CHB][hapmap] |
rs959690 | 1.00[CHB][hapmap] |
rs9628626 | 1.00[ASN][1000 genomes] |
rs9628634 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv548398 | chr1:185136458-186003094 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 69 gene(s) | inside rSNPs | diseases |
2 | esv3424090 | chr1:185679718-186270877 | Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:185730200-185745000 | Weak transcription | Fetal Kidney | kidney |
2 | chr1:185736000-185747000 | Weak transcription | Aorta | Aorta |
3 | chr1:185737000-185744600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
4 | chr1:185737800-185758800 | Weak transcription | Fetal Lung | lung |
5 | chr1:185742800-185744400 | Weak transcription | Fetal Heart | heart |
6 | chr1:185743200-185746000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
7 | chr1:185743600-185744400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
8 | chr1:185743600-185745000 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
9 | chr1:185743600-185745200 | Enhancers | HUES48 Cell Line | embryonic stem cell |
10 | chr1:185743600-185747000 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
11 | chr1:185743800-185744800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
12 | chr1:185743800-185744800 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
13 | chr1:185743800-185745400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
14 | chr1:185744000-185744600 | Strong transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
15 | chr1:185744000-185755000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |