Variant report
Variant | rs16873150 |
---|---|
Chromosome Location | chr6:45080058-45080059 |
allele | C/T |
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 |
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No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10080909 | 1.00[EUR][1000 genomes] |
rs16873056 | 0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs16873073 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16873103 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs16873215 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs17209608 | 1.00[CEU][hapmap] |
rs2396374 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs28463085 | 0.84[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs28877051 | 0.86[EUR][1000 genomes] |
rs34927422 | 0.85[EUR][1000 genomes] |
rs4582383 | 0.85[EUR][1000 genomes] |
rs58398217 | 0.85[EUR][1000 genomes] |
rs59379038 | 0.83[EUR][1000 genomes] |
rs6901579 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[EUR][1000 genomes] |
rs6912047 | 0.84[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs6925770 | 1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs73441120 | 0.88[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs73441122 | 0.88[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs73441130 | 0.85[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs73441184 | 0.85[EUR][1000 genomes] |
rs73442933 | 0.80[AFR][1000 genomes];0.81[EUR][1000 genomes] |
rs73443219 | 0.84[AFR][1000 genomes] |
rs73443229 | 0.84[AFR][1000 genomes] |
rs73443286 | 0.84[AFR][1000 genomes] |
rs73444966 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs73444983 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73447073 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs73447433 | 0.83[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs73451303 | 0.99[EUR][1000 genomes] |
rs7742332 | 1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7749796 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs7751298 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes] |
rs7762957 | 1.00[CEU][hapmap];0.96[EUR][1000 genomes] |
rs7764969 | 0.81[EUR][1000 genomes] |
rs9296450 | 1.00[YRI][hapmap] |
rs9296451 | 1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9463053 | 0.82[AFR][1000 genomes] |
rs9463056 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs9463058 | 1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9463066 | 1.00[CEU][hapmap] |
rs9463071 | 0.99[EUR][1000 genomes] |
rs9463079 | 0.84[AFR][1000 genomes];0.94[EUR][1000 genomes] |
rs9463080 | 0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs9463082 | 0.86[EUR][1000 genomes] |
rs9472412 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs9472413 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs9472414 | 1.00[YRI][hapmap] |
rs9472421 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs9472424 | 0.87[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs9472427 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs9472433 | 1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs9472434 | 1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9472435 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9472436 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9472438 | 1.00[CEU][hapmap] |
rs9472454 | 0.85[EUR][1000 genomes] |
rs9472455 | 0.86[EUR][1000 genomes] |
rs9472457 | 0.85[EUR][1000 genomes] |
rs9472458 | 0.82[EUR][1000 genomes] |
rs9885623 | 0.84[AFR][1000 genomes];0.84[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028393 | chr6:44875558-45822335 | Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
2 | nsv538211 | chr6:44875558-45822335 | ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
3 | nsv1024370 | chr6:44878053-45251451 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv885862 | chr6:44890760-45083966 | Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv885863 | chr6:44890760-45083966 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv885864 | chr6:44890760-45198796 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv1023018 | chr6:44925393-45152912 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
8 | nsv538212 | chr6:44925393-45152912 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv603008 | chr6:44958372-45081821 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
10 | nsv1026728 | chr6:45001948-45126730 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
11 | nsv538213 | chr6:45001948-45126730 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
12 | nsv885865 | chr6:45012223-45102025 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
13 | nsv492309 | chr6:45020402-45233484 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
14 | nsv528130 | chr6:45056086-45083966 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | nsv1032906 | chr6:45069368-45212863 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:45073400-45083600 | Weak transcription | Pancreas | Pancrea |
2 | chr6:45076600-45082800 | Weak transcription | Dnd41 | blood |
3 | chr6:45077800-45083400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
4 | chr6:45078400-45083400 | Weak transcription | HSMM | muscle |
5 | chr6:45079800-45080200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |