Variant report
Variant | rs12507399 |
---|---|
Chromosome Location | chr4:92280849-92280850 |
allele | A/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] |
---|---|
rs10516892 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs11938361 | 0.89[ASN][1000 genomes] |
rs11938470 | 0.89[ASN][1000 genomes] |
rs12186312 | 0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap] |
rs12498254 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12507382 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12507411 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12511436 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1547594 | 0.84[CEU][hapmap] |
rs17018388 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17214010 | 0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs1830354 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2141397 | 0.95[CEU][hapmap];1.00[JPT][hapmap] |
rs2870310 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs34594961 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4096930 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4096931 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4128703 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4128704 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4128705 | 0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4411947 | 0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6829492 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs72880824 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72880827 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72880830 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869023 | chr4:91940838-92935383 | Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | esv3384271 | chr4:92073391-92464275 | Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv879566 | chr4:92215966-92322333 | ZNF genes & repeats Enhancers Weak transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv879567 | chr4:92215966-92413671 | ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
5 | nsv522208 | chr4:92241587-92283771 | ZNF genes & repeats Enhancers Weak transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | esv1830673 | chr4:92241587-92379081 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
7 | nsv879568 | chr4:92244300-92429961 | Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
8 | nsv529020 | chr4:92253926-92293482 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv594849 | chr4:92271993-92285150 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
10 | nsv966558 | chr4:92273882-92285480 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:92279800-92281000 | Enhancers | Rectal Mucosa Donor 31 | rectum |