Variant report
Variant | rs57967341 |
---|---|
Chromosome Location | chr1:224540747-224540748 |
allele | C/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] |
---|---|
rs10495221 | 1.00[EUR][1000 genomes] |
rs11801211 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11802182 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11807149 | 1.00[EUR][1000 genomes] |
rs11809688 | 1.00[EUR][1000 genomes] |
rs11809710 | 1.00[EUR][1000 genomes] |
rs11810160 | 1.00[EUR][1000 genomes] |
rs11811935 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11812007 | 1.00[EUR][1000 genomes] |
rs12239235 | 1.00[EUR][1000 genomes] |
rs12239466 | 1.00[EUR][1000 genomes] |
rs1401319 | 1.00[EUR][1000 genomes] |
rs1499284 | 1.00[EUR][1000 genomes] |
rs16845729 | 1.00[AMR][1000 genomes] |
rs16845878 | 1.00[AMR][1000 genomes] |
rs16846190 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16846212 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16846293 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16846339 | 0.81[AFR][1000 genomes] |
rs16846494 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16847675 | 1.00[EUR][1000 genomes] |
rs16847784 | 1.00[EUR][1000 genomes] |
rs16847858 | 1.00[EUR][1000 genomes] |
rs16847870 | 1.00[EUR][1000 genomes] |
rs16847871 | 1.00[EUR][1000 genomes] |
rs16849419 | 1.00[EUR][1000 genomes] |
rs16849547 | 1.00[EUR][1000 genomes] |
rs1857042 | 1.00[EUR][1000 genomes] |
rs2068945 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2794805 | 1.00[EUR][1000 genomes] |
rs4653586 | 1.00[EUR][1000 genomes] |
rs55712053 | 1.00[EUR][1000 genomes] |
rs57027684 | 1.00[AMR][1000 genomes] |
rs57469223 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57719044 | 1.00[EUR][1000 genomes] |
rs58304668 | 1.00[EUR][1000 genomes] |
rs58649883 | 1.00[EUR][1000 genomes] |
rs58788859 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58814229 | 1.00[EUR][1000 genomes] |
rs58954846 | 1.00[EUR][1000 genomes] |
rs59034185 | 1.00[EUR][1000 genomes] |
rs59236258 | 1.00[AMR][1000 genomes] |
rs59561838 | 1.00[EUR][1000 genomes] |
rs59577766 | 1.00[EUR][1000 genomes] |
rs59710928 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60349703 | 1.00[EUR][1000 genomes] |
rs60627429 | 1.00[EUR][1000 genomes] |
rs60715845 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60831135 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61000820 | 1.00[EUR][1000 genomes] |
rs61155217 | 1.00[EUR][1000 genomes] |
rs61162360 | 1.00[EUR][1000 genomes] |
rs61278437 | 1.00[EUR][1000 genomes] |
rs6426167 | 1.00[EUR][1000 genomes] |
rs6658918 | 1.00[EUR][1000 genomes] |
rs6659109 | 1.00[EUR][1000 genomes] |
rs6674133 | 1.00[EUR][1000 genomes] |
rs6681611 | 1.00[EUR][1000 genomes] |
rs6687424 | 1.00[EUR][1000 genomes] |
rs6691181 | 1.00[EUR][1000 genomes] |
rs6702649 | 1.00[EUR][1000 genomes] |
rs73121865 | 1.00[EUR][1000 genomes] |
rs73123788 | 1.00[EUR][1000 genomes] |
rs73123791 | 1.00[EUR][1000 genomes] |
rs73124468 | 1.00[EUR][1000 genomes] |
rs73124491 | 1.00[EUR][1000 genomes] |
rs73124493 | 1.00[EUR][1000 genomes] |
rs73125526 | 1.00[EUR][1000 genomes] |
rs73125529 | 1.00[EUR][1000 genomes] |
rs73126411 | 1.00[EUR][1000 genomes] |
rs73128442 | 1.00[EUR][1000 genomes] |
rs73133345 | 1.00[EUR][1000 genomes] |
rs74146372 | 1.00[EUR][1000 genomes] |
rs74146374 | 1.00[EUR][1000 genomes] |
rs74146377 | 1.00[EUR][1000 genomes] |
rs74146381 | 1.00[EUR][1000 genomes] |
rs74146382 | 1.00[EUR][1000 genomes] |
rs74146383 | 1.00[EUR][1000 genomes] |
rs74146384 | 1.00[EUR][1000 genomes] |
rs74146386 | 1.00[EUR][1000 genomes] |
rs74146389 | 1.00[EUR][1000 genomes] |
rs7512165 | 1.00[EUR][1000 genomes] |
rs9661679 | 1.00[EUR][1000 genomes] |
rs9661938 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv8868 | chr1:224383023-224752531 | Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
2 | nsv469889 | chr1:224440354-224634374 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
3 | nsv482318 | chr1:224440354-224634374 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:224529200-224544000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
2 | chr1:224536800-224541400 | Weak transcription | Primary T cells from cord blood | blood |
3 | chr1:224536800-224544200 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
4 | chr1:224536800-224544400 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
5 | chr1:224536800-224544600 | Weak transcription | Primary T killer memory cells from peripheral blood | blood |
6 | chr1:224538400-224544400 | Weak transcription | Right Atrium | heart |
7 | chr1:224540200-224540800 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
8 | chr1:224540400-224540800 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
9 | chr1:224540600-224540800 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
10 | chr1:224540600-224544400 | Enhancers | Fetal Intestine Small | intestine |