Variant report
Variant | rs978754 |
---|---|
Chromosome Location | chr1:210213891-210213892 |
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] |
---|---|
rs1002383 | 0.83[AMR][1000 genomes] |
rs10127635 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1016480 | 1.00[EUR][1000 genomes] |
rs1016481 | 1.00[EUR][1000 genomes] |
rs10863808 | 1.00[EUR][1000 genomes] |
rs11119380 | 1.00[EUR][1000 genomes] |
rs11119393 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11119395 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11119397 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs11119402 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11119404 | 1.00[EUR][1000 genomes] |
rs11119405 | 0.94[AMR][1000 genomes] |
rs11119408 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11119411 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11801400 | 1.00[EUR][1000 genomes] |
rs11810848 | 1.00[EUR][1000 genomes] |
rs11811996 | 1.00[EUR][1000 genomes] |
rs12059259 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12073806 | 1.00[EUR][1000 genomes] |
rs12078871 | 1.00[EUR][1000 genomes] |
rs12079711 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12080332 | 1.00[EUR][1000 genomes] |
rs12082067 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12085355 | 1.00[EUR][1000 genomes] |
rs12086145 | 1.00[EUR][1000 genomes] |
rs12088415 | 1.00[EUR][1000 genomes] |
rs12089636 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12090781 | 1.00[EUR][1000 genomes] |
rs12092551 | 1.00[EUR][1000 genomes] |
rs12093254 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12239153 | 0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12239590 | 1.00[EUR][1000 genomes] |
rs12239724 | 1.00[EUR][1000 genomes] |
rs1334572 | 1.00[EUR][1000 genomes] |
rs13376651 | 1.00[EUR][1000 genomes] |
rs1413698 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1591300 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1602289 | 1.00[EUR][1000 genomes] |
rs17015476 | 1.00[EUR][1000 genomes] |
rs17015480 | 1.00[EUR][1000 genomes] |
rs17015532 | 1.00[EUR][1000 genomes] |
rs17015561 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17015638 | 1.00[EUR][1000 genomes] |
rs17015652 | 1.00[EUR][1000 genomes] |
rs17041975 | 1.00[EUR][1000 genomes] |
rs2018942 | 1.00[EUR][1000 genomes] |
rs2130626 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2130627 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2130628 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2171988 | 1.00[EUR][1000 genomes] |
rs34400113 | 1.00[EUR][1000 genomes] |
rs35046399 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56075770 | 1.00[EUR][1000 genomes] |
rs56105015 | 1.00[EUR][1000 genomes] |
rs56271040 | 1.00[EUR][1000 genomes] |
rs56733441 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57082045 | 1.00[EUR][1000 genomes] |
rs57790572 | 1.00[EUR][1000 genomes] |
rs58775140 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59230578 | 1.00[EUR][1000 genomes] |
rs59254815 | 0.89[AMR][1000 genomes] |
rs59904008 | 0.90[AFR][1000 genomes];0.94[AMR][1000 genomes] |
rs61049229 | 1.00[EUR][1000 genomes] |
rs6540577 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6689269 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6692116 | 1.00[EUR][1000 genomes] |
rs6692822 | 1.00[EUR][1000 genomes] |
rs73066422 | 1.00[EUR][1000 genomes] |
rs73066498 | 1.00[EUR][1000 genomes] |
rs73068419 | 1.00[EUR][1000 genomes] |
rs73072224 | 1.00[EUR][1000 genomes] |
rs74156109 | 1.00[EUR][1000 genomes] |
rs74156117 | 1.00[EUR][1000 genomes] |
rs74156272 | 1.00[EUR][1000 genomes] |
rs7512760 | 1.00[EUR][1000 genomes] |
rs7515629 | 1.00[EUR][1000 genomes] |
rs7523089 | 1.00[EUR][1000 genomes] |
rs7530907 | 1.00[EUR][1000 genomes] |
rs7536495 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7556078 | 1.00[EUR][1000 genomes] |
rs970788 | 1.00[EUR][1000 genomes] |
rs9803620 | 1.00[EUR][1000 genomes] |
rs9970894 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014034 | chr1:209759648-210501731 | Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 45 gene(s) | inside rSNPs | diseases |
2 | nsv873140 | chr1:210068117-210335644 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | esv1821002 | chr1:210108473-210291476 | ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:210193400-210221000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr1:210195000-210221200 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
3 | chr1:210212000-210215600 | Strong transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr1:210212600-210215000 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr1:210213000-210221800 | Weak transcription | Brain Germinal Matrix | brain |
6 | chr1:210213000-210223800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |