Variant report
Variant | rs11801400 |
---|---|
Chromosome Location | chr1:210110377-210110378 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:2 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | JUND | chr1:210110209-210112774 | SK-N-SH | brain: | n/a | chr1:210111772-210111781 |
2 | MXI1 | chr1:210110276-210113314 | SK-N-SH | brain: | n/a | n/a |
No data |
No data |
(count:1 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-IRF6-1 | chr1:210107873-210111294 | NONHSAT009248 |
No data |
No data |
Variant related genes | Relation type |
---|---|
SYT14 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10127635 | 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 | 1.00[EUR][1000 genomes] |
rs11119395 | 1.00[EUR][1000 genomes] |
rs11119402 | 1.00[EUR][1000 genomes] |
rs11119404 | 1.00[EUR][1000 genomes] |
rs11119408 | 1.00[EUR][1000 genomes] |
rs11119411 | 1.00[EUR][1000 genomes] |
rs11810848 | 1.00[EUR][1000 genomes] |
rs11811996 | 1.00[EUR][1000 genomes] |
rs12059259 | 1.00[EUR][1000 genomes] |
rs12073806 | 1.00[EUR][1000 genomes] |
rs12078871 | 1.00[EUR][1000 genomes] |
rs12079711 | 1.00[EUR][1000 genomes] |
rs12080332 | 1.00[EUR][1000 genomes] |
rs12082067 | 1.00[EUR][1000 genomes] |
rs12085355 | 1.00[EUR][1000 genomes] |
rs12086145 | 1.00[EUR][1000 genomes] |
rs12089636 | 1.00[EUR][1000 genomes] |
rs12090781 | 1.00[EUR][1000 genomes] |
rs12092551 | 1.00[EUR][1000 genomes] |
rs12093254 | 1.00[EUR][1000 genomes] |
rs12239153 | 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 | 1.00[EUR][1000 genomes] |
rs1591300 | 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 | 1.00[EUR][1000 genomes] |
rs17015638 | 1.00[EUR][1000 genomes] |
rs17015652 | 1.00[EUR][1000 genomes] |
rs17041975 | 1.00[EUR][1000 genomes] |
rs2018942 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2130626 | 1.00[EUR][1000 genomes] |
rs2130627 | 1.00[EUR][1000 genomes] |
rs2130628 | 1.00[EUR][1000 genomes] |
rs2171988 | 1.00[EUR][1000 genomes] |
rs34400113 | 1.00[EUR][1000 genomes] |
rs35046399 | 1.00[EUR][1000 genomes] |
rs56075770 | 1.00[EUR][1000 genomes] |
rs56105015 | 1.00[EUR][1000 genomes] |
rs56271040 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56733441 | 1.00[EUR][1000 genomes] |
rs57082045 | 1.00[EUR][1000 genomes] |
rs57160562 | 0.87[AMR][1000 genomes] |
rs57790572 | 1.00[EUR][1000 genomes] |
rs58775140 | 1.00[EUR][1000 genomes] |
rs59230578 | 1.00[EUR][1000 genomes] |
rs61049229 | 1.00[EUR][1000 genomes] |
rs61644695 | 0.89[AMR][1000 genomes] |
rs6540577 | 1.00[EUR][1000 genomes] |
rs6689269 | 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] |
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 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7531737 | 0.87[AMR][1000 genomes] |
rs7536495 | 1.00[EUR][1000 genomes] |
rs7556078 | 1.00[EUR][1000 genomes] |
rs970788 | 1.00[EUR][1000 genomes] |
rs978754 | 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 | nsv999901 | chr1:209600631-210205379 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 76 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | 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 |
4 | esv1825811 | chr1:210082206-210135806 | Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | 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 |
6 | esv3438109 | chr1:210110354-210112902 | Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:210110200-210110400 | Enhancers | Brain Dorsolateral Prefrontal Cortex | brain |
2 | chr1:210110200-210110400 | Flanking Active TSS | Pancreatic Islets | Pancreatic Islet |
3 | chr1:210110200-210110600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr1:210110200-210112400 | Active TSS | Brain Anterior Caudate | brain |
5 | chr1:210110200-210112800 | Active TSS | Brain Angular Gyrus | brain |