Variant report
Variant | rs2082553 |
---|---|
Chromosome Location | chr4:94301291-94301292 |
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] |
---|---|
rs10001043 | 0.80[EUR][1000 genomes] |
rs10002068 | 0.91[EUR][1000 genomes] |
rs10002534 | 0.95[EUR][1000 genomes] |
rs10003805 | 0.85[EUR][1000 genomes] |
rs10010189 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10012783 | 0.81[EUR][1000 genomes] |
rs10015087 | 0.81[EUR][1000 genomes] |
rs10019237 | 0.85[EUR][1000 genomes] |
rs10022114 | 0.81[EUR][1000 genomes] |
rs10034637 | 0.81[EUR][1000 genomes] |
rs11937272 | 0.81[EUR][1000 genomes] |
rs1485022 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1485024 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17020544 | 0.81[EUR][1000 genomes] |
rs17020556 | 0.81[EUR][1000 genomes] |
rs17020658 | 0.85[EUR][1000 genomes] |
rs17272388 | 1.00[EUR][1000 genomes] |
rs17330789 | 1.00[EUR][1000 genomes] |
rs1905707 | 0.81[EUR][1000 genomes] |
rs1905708 | 0.81[EUR][1000 genomes] |
rs1905709 | 0.81[EUR][1000 genomes] |
rs1948018 | 0.81[EUR][1000 genomes] |
rs1994252 | 0.81[EUR][1000 genomes] |
rs28480348 | 0.81[EUR][1000 genomes] |
rs28578392 | 0.82[EUR][1000 genomes] |
rs28683046 | 0.81[EUR][1000 genomes] |
rs28715682 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs28768784 | 0.81[EUR][1000 genomes] |
rs6532406 | 0.81[EUR][1000 genomes] |
rs6820920 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6826128 | 0.82[EUR][1000 genomes] |
rs6827657 | 0.82[EUR][1000 genomes] |
rs6854722 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs72884566 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72886217 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs733941 | 0.93[EUR][1000 genomes] |
rs9307124 | 0.85[EUR][1000 genomes] |
rs9790383 | 0.81[EUR][1000 genomes] |
rs9992229 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1013255 | chr4:94027129-94462345 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv2830401 | chr4:94141655-94450106 | Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv3584808 | chr4:94156602-94559327 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1008055 | chr4:94169131-95030074 | Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv533846 | chr4:94264488-94462921 | Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv931979 | chr4:94289958-95121723 | Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:94296400-94304200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |