Variant report
Variant | rs13374655 |
---|---|
Chromosome Location | chr1:215567160-215567161 |
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] |
---|---|
rs10127809 | 0.97[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs10465665 | 0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10864176 | 1.00[EUR][1000 genomes] |
rs11120520 | 1.00[EUR][1000 genomes] |
rs11120521 | 1.00[EUR][1000 genomes] |
rs11120523 | 1.00[EUR][1000 genomes] |
rs11120553 | 1.00[EUR][1000 genomes] |
rs11120555 | 1.00[EUR][1000 genomes] |
rs11120556 | 1.00[EUR][1000 genomes] |
rs11120570 | 1.00[EUR][1000 genomes] |
rs11120571 | 1.00[EUR][1000 genomes] |
rs11120572 | 1.00[EUR][1000 genomes] |
rs11120573 | 1.00[EUR][1000 genomes] |
rs11120574 | 1.00[EUR][1000 genomes] |
rs12061570 | 1.00[EUR][1000 genomes] |
rs12070211 | 1.00[EUR][1000 genomes] |
rs12074526 | 1.00[EUR][1000 genomes] |
rs12076291 | 1.00[EUR][1000 genomes] |
rs12076683 | 1.00[EUR][1000 genomes] |
rs12077050 | 1.00[EUR][1000 genomes] |
rs12077731 | 1.00[EUR][1000 genomes] |
rs12077775 | 1.00[EUR][1000 genomes] |
rs12078628 | 1.00[EUR][1000 genomes] |
rs12079873 | 1.00[EUR][1000 genomes] |
rs12080017 | 1.00[EUR][1000 genomes] |
rs12094048 | 1.00[EUR][1000 genomes] |
rs12095159 | 1.00[EUR][1000 genomes] |
rs12239472 | 1.00[EUR][1000 genomes] |
rs12239509 | 1.00[EUR][1000 genomes] |
rs13374480 | 1.00[EUR][1000 genomes] |
rs1416650 | 1.00[EUR][1000 genomes] |
rs1556904 | 1.00[EUR][1000 genomes] |
rs17024391 | 1.00[EUR][1000 genomes] |
rs17024744 | 0.97[AFR][1000 genomes] |
rs17024751 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17024755 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs17024758 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs17024855 | 1.00[EUR][1000 genomes] |
rs1911547 | 1.00[EUR][1000 genomes] |
rs35134381 | 0.96[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs4082520 | 1.00[EUR][1000 genomes] |
rs4082521 | 1.00[EUR][1000 genomes] |
rs4265403 | 1.00[EUR][1000 genomes] |
rs4593794 | 1.00[EUR][1000 genomes] |
rs4607849 | 0.97[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs4633260 | 1.00[EUR][1000 genomes] |
rs5019190 | 1.00[EUR][1000 genomes] |
rs56799360 | 1.00[EUR][1000 genomes] |
rs57309511 | 0.98[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs57501351 | 1.00[EUR][1000 genomes] |
rs59473177 | 1.00[EUR][1000 genomes] |
rs60597792 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61070702 | 1.00[EUR][1000 genomes] |
rs61272547 | 1.00[EUR][1000 genomes] |
rs6678266 | 1.00[EUR][1000 genomes] |
rs6690170 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6695816 | 1.00[EUR][1000 genomes] |
rs73091976 | 0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73091981 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73091984 | 1.00[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs73091986 | 1.00[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs73091996 | 1.00[EUR][1000 genomes] |
rs7516768 | 1.00[EUR][1000 genomes] |
rs950987 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832537 | chr1:215509026-215705105 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | esv1796390 | chr1:215561548-215799074 | Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:215563400-215568000 | Weak transcription | H1 Cell Line | embryonic stem cell |
2 | chr1:215565400-215567400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr1:215567000-215567400 | Enhancers | Cortex derived primary cultured neurospheres | brain |