Variant report
Variant | rs4982487 |
---|---|
Chromosome Location | chr14:22169400-22169401 |
allele | G/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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10148566 | 0.89[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes] |
rs10151114 | 0.95[CHD][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes] |
rs12431503 | 0.85[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap] |
rs12434471 | 1.00[CEU][hapmap];0.93[JPT][hapmap];0.91[YRI][hapmap] |
rs12589185 | 0.95[CHD][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes] |
rs12589513 | 1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap] |
rs12589962 | 0.85[JPT][hapmap];0.82[ASN][1000 genomes] |
rs12894518 | 0.85[JPT][hapmap];0.85[ASN][1000 genomes] |
rs17182761 | 0.95[CHD][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes] |
rs2319874 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2319875 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs28575550 | 0.95[CHD][hapmap];0.85[JPT][hapmap] |
rs35762321 | 0.82[EUR][1000 genomes] |
rs4513011 | 0.81[ASN][1000 genomes] |
rs4628878 | 0.85[JPT][hapmap];0.82[ASN][1000 genomes] |
rs4982486 | 1.00[ASW][hapmap];0.87[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap] |
rs55654479 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs59305233 | 0.91[AFR][1000 genomes] |
rs6650488 | 0.85[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs7143458 | 0.94[JPT][hapmap] |
rs7143695 | 0.88[ASN][1000 genomes] |
rs7148008 | 1.00[JPT][hapmap] |
rs7158141 | 0.82[ASN][1000 genomes] |
rs725891 | 0.82[MEX][hapmap];0.80[TSI][hapmap];0.96[YRI][hapmap] |
rs72688056 | 0.91[AFR][1000 genomes] |
rs8016911 | 0.81[ASN][1000 genomes] |
rs8017708 | 0.91[YRI][hapmap] |
rs8020038 | 0.87[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap] |
rs8020165 | 0.83[CHB][hapmap];1.00[JPT][hapmap] |
rs8022425 | 1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2422459 | chr14:21931624-22169502 | Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
2 | nsv1042309 | chr14:22042511-22866936 | Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 90 gene(s) | inside rSNPs | diseases |
3 | nsv456147 | chr14:22073473-22305071 | Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
4 | nsv563851 | chr14:22073473-22305071 | Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
5 | nsv510629 | chr14:22134425-22215842 | Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:22168600-22169800 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
2 | chr14:22169000-22171000 | Weak transcription | Rectal Mucosa Donor 29 | rectum |