Variant report
Variant | rs12036690 |
---|---|
Chromosome Location | chr1:80014528-80014529 |
allele | C/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] |
---|---|
rs10874038 | 0.83[EUR][1000 genomes] |
rs12023367 | 1.00[AFR][1000 genomes] |
rs12025658 | 1.00[AFR][1000 genomes] |
rs12026767 | 1.00[AFR][1000 genomes] |
rs12027888 | 1.00[AFR][1000 genomes] |
rs12029642 | 1.00[AFR][1000 genomes] |
rs12030013 | 1.00[AFR][1000 genomes] |
rs12034665 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs12036905 | 0.83[EUR][1000 genomes] |
rs12039488 | 1.00[AFR][1000 genomes] |
rs12039867 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs12039923 | 0.83[EUR][1000 genomes] |
rs12040033 | 1.00[AFR][1000 genomes] |
rs12040237 | 0.83[EUR][1000 genomes] |
rs12040880 | 0.83[EUR][1000 genomes] |
rs12041108 | 1.00[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs12041180 | 1.00[AFR][1000 genomes] |
rs12041732 | 1.00[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs12041849 | 1.00[AFR][1000 genomes] |
rs12042159 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs12043955 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs12044515 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs12044901 | 1.00[AFR][1000 genomes] |
rs12045663 | 0.83[EUR][1000 genomes] |
rs12045991 | 0.83[EUR][1000 genomes] |
rs12047490 | 0.82[CHB][hapmap];1.00[AFR][1000 genomes] |
rs1603126 | 0.88[ASN][1000 genomes] |
rs17098662 | 1.00[AFR][1000 genomes] |
rs17103209 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs17103224 | 1.00[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs17103273 | 1.00[AFR][1000 genomes] |
rs17103305 | 1.00[AFR][1000 genomes] |
rs2088103 | 0.83[EUR][1000 genomes] |
rs2132054 | 0.83[EUR][1000 genomes] |
rs3000143 | 0.83[EUR][1000 genomes] |
rs3000144 | 0.83[EUR][1000 genomes] |
rs3000145 | 0.83[EUR][1000 genomes] |
rs3015018 | 0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1004014 | chr1:79811049-80042309 | Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1012004 | chr1:79945395-80096748 | Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv535017 | chr1:79945395-80096748 | Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1012296 | chr1:79945395-80300216 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1005022 | chr1:79950774-80106902 | Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv546636 | chr1:79964823-80079996 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv546637 | chr1:79984748-80159969 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:80014400-80015400 | Enhancers | Fetal Muscle Leg | muscle |