Variant report
Variant | rs73968415 |
---|---|
Chromosome Location | chr2:100962287-100962288 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:100958458..100960134-chr2:100961869..100964277,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10167159 | 0.94[ASN][1000 genomes] |
rs10180570 | 0.82[ASN][1000 genomes] |
rs10184899 | 0.82[ASN][1000 genomes] |
rs10193535 | 0.82[ASN][1000 genomes] |
rs10198495 | 0.94[ASN][1000 genomes] |
rs10198682 | 0.94[ASN][1000 genomes] |
rs10200480 | 0.94[ASN][1000 genomes] |
rs10201098 | 0.94[ASN][1000 genomes] |
rs10204833 | 0.94[ASN][1000 genomes] |
rs10206374 | 0.82[ASN][1000 genomes] |
rs10208900 | 0.94[ASN][1000 genomes] |
rs10208911 | 0.94[ASN][1000 genomes] |
rs10209186 | 0.94[ASN][1000 genomes] |
rs1107429 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs13391930 | 0.82[ASN][1000 genomes] |
rs13396147 | 0.82[ASN][1000 genomes] |
rs13404823 | 0.82[ASN][1000 genomes] |
rs13407408 | 0.82[ASN][1000 genomes] |
rs13407648 | 0.82[ASN][1000 genomes] |
rs13407891 | 0.82[ASN][1000 genomes] |
rs13410582 | 0.82[ASN][1000 genomes] |
rs13419808 | 0.82[ASN][1000 genomes] |
rs13420942 | 0.94[ASN][1000 genomes] |
rs1347721 | 0.82[ASN][1000 genomes] |
rs1370627 | 0.94[ASN][1000 genomes] |
rs1437970 | 0.94[ASN][1000 genomes] |
rs17023985 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs17024035 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs17024129 | 0.82[ASN][1000 genomes] |
rs17024136 | 0.82[ASN][1000 genomes] |
rs17024144 | 0.82[ASN][1000 genomes] |
rs1898571 | 0.82[ASN][1000 genomes] |
rs1898574 | 0.94[ASN][1000 genomes] |
rs2309793 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs55640826 | 0.82[ASN][1000 genomes] |
rs55843950 | 0.82[ASN][1000 genomes] |
rs56051859 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs56118658 | 0.82[ASN][1000 genomes] |
rs56342384 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs56656536 | 0.82[ASN][1000 genomes] |
rs58876304 | 0.82[ASN][1000 genomes] |
rs60131548 | 0.82[ASN][1000 genomes] |
rs60609848 | 0.82[ASN][1000 genomes] |
rs60898093 | 0.82[ASN][1000 genomes] |
rs61321970 | 0.94[ASN][1000 genomes] |
rs6542931 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6542932 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6542939 | 0.94[ASN][1000 genomes] |
rs6542941 | 0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6708942 | 0.82[ASN][1000 genomes] |
rs6713862 | 0.82[ASN][1000 genomes] |
rs6714109 | 0.94[ASN][1000 genomes] |
rs6716009 | 0.82[ASN][1000 genomes] |
rs6716367 | 0.82[ASN][1000 genomes] |
rs6724695 | 0.82[ASN][1000 genomes] |
rs6732285 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6739576 | 0.94[ASN][1000 genomes] |
rs6740098 | 0.94[ASN][1000 genomes] |
rs6750866 | 0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6754379 | 0.94[ASN][1000 genomes] |
rs6755395 | 0.94[ASN][1000 genomes] |
rs6757774 | 0.82[ASN][1000 genomes] |
rs6758156 | 0.82[ASN][1000 genomes] |
rs6758161 | 0.82[ASN][1000 genomes] |
rs6758515 | 0.82[ASN][1000 genomes] |
rs6761561 | 0.82[ASN][1000 genomes] |
rs72960172 | 0.94[ASN][1000 genomes] |
rs72960184 | 0.82[ASN][1000 genomes] |
rs72960186 | 0.82[ASN][1000 genomes] |
rs72960202 | 0.82[ASN][1000 genomes] |
rs73966107 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs73966108 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs73968412 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs73968817 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs7556717 | 0.94[ASN][1000 genomes] |
rs7557137 | 0.94[ASN][1000 genomes] |
rs7559939 | 0.82[ASN][1000 genomes] |
rs7559946 | 0.82[ASN][1000 genomes] |
rs7562461 | 0.82[ASN][1000 genomes] |
rs7562479 | 0.82[ASN][1000 genomes] |
rs7562486 | 0.82[ASN][1000 genomes] |
rs7562615 | 0.82[ASN][1000 genomes] |
rs7564178 | 0.82[ASN][1000 genomes] |
rs7572119 | 0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7574684 | 0.82[ASN][1000 genomes] |
rs7576749 | 0.82[ASN][1000 genomes] |
rs7585898 | 0.82[ASN][1000 genomes] |
rs7587333 | 0.82[ASN][1000 genomes] |
rs7597631 | 0.94[ASN][1000 genomes] |
rs7597722 | 0.94[ASN][1000 genomes] |
rs7606723 | 0.94[ASN][1000 genomes] |
rs9308834 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1007777 | chr2:100816913-101308914 | Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
2 | nsv535844 | chr2:100816913-101308914 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
3 | nsv834311 | chr2:100816917-100990036 | Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
4 | nsv582531 | chr2:100908508-101207639 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:100956800-100967200 | Weak transcription | Gastric | stomach |
2 | chr2:100961200-100963400 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |