Variant report
Variant | rs16945946 |
---|---|
Chromosome Location | chr16:48242359-48242360 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000121270 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs16945857 | 1.00[AMR][1000 genomes] |
rs16945864 | 1.00[AMR][1000 genomes] |
rs16945867 | 1.00[AMR][1000 genomes] |
rs16945872 | 1.00[AMR][1000 genomes] |
rs16945876 | 1.00[AMR][1000 genomes] |
rs16945878 | 1.00[AMR][1000 genomes] |
rs16945880 | 1.00[AMR][1000 genomes] |
rs16945881 | 1.00[AMR][1000 genomes] |
rs16945883 | 1.00[AMR][1000 genomes] |
rs16945890 | 1.00[AMR][1000 genomes] |
rs16945892 | 1.00[AMR][1000 genomes] |
rs16945895 | 1.00[AMR][1000 genomes] |
rs16945897 | 1.00[AMR][1000 genomes] |
rs16945901 | 1.00[AMR][1000 genomes] |
rs16945903 | 1.00[AMR][1000 genomes] |
rs16945904 | 1.00[AMR][1000 genomes] |
rs16945922 | 1.00[AMR][1000 genomes] |
rs16945926 | 1.00[AMR][1000 genomes] |
rs16945943 | 1.00[AMR][1000 genomes] |
rs16946016 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs16946018 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs16946020 | 0.85[AFR][1000 genomes] |
rs16946022 | 0.85[AFR][1000 genomes] |
rs16946024 | 0.85[AFR][1000 genomes] |
rs16946028 | 0.85[AFR][1000 genomes] |
rs16946031 | 0.85[AFR][1000 genomes] |
rs16946033 | 0.85[AFR][1000 genomes] |
rs16946106 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap] |
rs16946120 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap] |
rs17815694 | 1.00[AMR][1000 genomes] |
rs2160564 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes] |
rs2353650 | 1.00[ASW][hapmap];0.91[LWK][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes] |
rs34437640 | 1.00[ASW][hapmap];1.00[LWK][hapmap];0.88[YRI][hapmap] |
rs35730749 | 1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap] |
rs55913020 | 1.00[AMR][1000 genomes] |
rs55939380 | 0.85[AFR][1000 genomes] |
rs56006148 | 0.85[AFR][1000 genomes] |
rs56039807 | 0.85[AFR][1000 genomes] |
rs56068904 | 0.85[AFR][1000 genomes] |
rs56210528 | 0.85[AFR][1000 genomes] |
rs56252717 | 0.81[AFR][1000 genomes] |
rs57045758 | 0.85[AFR][1000 genomes] |
rs57646139 | 0.81[AFR][1000 genomes] |
rs57858756 | 0.81[AFR][1000 genomes] |
rs58041814 | 1.00[AMR][1000 genomes] |
rs58068024 | 0.85[AFR][1000 genomes] |
rs58095119 | 0.81[AFR][1000 genomes] |
rs58315149 | 0.85[AFR][1000 genomes] |
rs58405777 | 0.85[AFR][1000 genomes] |
rs58531648 | 0.81[AFR][1000 genomes] |
rs58952249 | 0.85[AFR][1000 genomes] |
rs59000493 | 1.00[AMR][1000 genomes] |
rs59077393 | 0.85[AFR][1000 genomes] |
rs59174783 | 0.81[AFR][1000 genomes] |
rs59295735 | 0.85[AFR][1000 genomes] |
rs59382226 | 0.85[AFR][1000 genomes] |
rs59404336 | 1.00[AMR][1000 genomes] |
rs59546442 | 1.00[AMR][1000 genomes] |
rs59815620 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60438421 | 1.00[AMR][1000 genomes] |
rs60752576 | 1.00[AMR][1000 genomes] |
rs60791230 | 0.85[AFR][1000 genomes] |
rs61055548 | 0.85[AFR][1000 genomes] |
rs61695297 | 1.00[AMR][1000 genomes] |
rs7184973 | 1.00[AMR][1000 genomes] |
rs7187621 | 1.00[AMR][1000 genomes] |
rs7197710 | 1.00[AMR][1000 genomes] |
rs7204946 | 1.00[AMR][1000 genomes] |
rs74016323 | 0.85[AFR][1000 genomes] |
rs74016324 | 0.85[AFR][1000 genomes] |
rs74016326 | 0.85[AFR][1000 genomes] |
rs74016331 | 0.85[AFR][1000 genomes] |
rs74016334 | 0.85[AFR][1000 genomes] |
rs74016335 | 0.85[AFR][1000 genomes] |
rs74016337 | 0.85[AFR][1000 genomes] |
rs74016338 | 0.85[AFR][1000 genomes] |
rs74016339 | 0.85[AFR][1000 genomes] |
rs74016340 | 0.85[AFR][1000 genomes] |
rs74016341 | 0.85[AFR][1000 genomes] |
rs74016342 | 0.85[AFR][1000 genomes] |
rs74016343 | 0.85[AFR][1000 genomes] |
rs74016344 | 0.85[AFR][1000 genomes] |
rs74016345 | 0.85[AFR][1000 genomes] |
rs74016346 | 0.85[AFR][1000 genomes] |
rs74016347 | 0.85[AFR][1000 genomes] |
rs74016348 | 0.85[AFR][1000 genomes] |
rs74016349 | 0.85[AFR][1000 genomes] |
rs74016350 | 0.85[AFR][1000 genomes] |
rs74016351 | 0.85[AFR][1000 genomes] |
rs74016352 | 0.82[AFR][1000 genomes] |
rs74016353 | 0.85[AFR][1000 genomes] |
rs74016355 | 0.85[AFR][1000 genomes] |
rs74016357 | 0.85[AFR][1000 genomes] |
rs74016358 | 0.85[AFR][1000 genomes] |
rs74018257 | 1.00[AMR][1000 genomes] |
rs74018258 | 1.00[AMR][1000 genomes] |
rs74018260 | 1.00[AMR][1000 genomes] |
rs74018262 | 1.00[AMR][1000 genomes] |
rs74018265 | 1.00[AMR][1000 genomes] |
rs74018274 | 1.00[AMR][1000 genomes] |
rs74018275 | 1.00[AMR][1000 genomes] |
rs74018276 | 1.00[AMR][1000 genomes] |
rs74018277 | 1.00[AMR][1000 genomes] |
rs74018278 | 1.00[AMR][1000 genomes] |
rs74018281 | 1.00[AMR][1000 genomes] |
rs74018285 | 1.00[AMR][1000 genomes] |
rs74018286 | 1.00[AMR][1000 genomes] |
rs74018287 | 1.00[AMR][1000 genomes] |
rs74018289 | 1.00[AMR][1000 genomes] |
rs74018292 | 1.00[AMR][1000 genomes] |
rs74018293 | 1.00[AMR][1000 genomes] |
rs74018294 | 1.00[AMR][1000 genomes] |
rs74018296 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1059259 | chr16:48113396-48304404 | Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv542916 | chr16:48113396-48304404 | Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:48239400-48245800 | Weak transcription | Right Atrium | heart |
2 | chr16:48239600-48250000 | Weak transcription | Pancreas | Pancrea |
3 | chr16:48241000-48245800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
4 | chr16:48241200-48243400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
5 | chr16:48241200-48244000 | Weak transcription | Liver | Liver |
6 | chr16:48241200-48244400 | Weak transcription | HMEC | breast |
7 | chr16:48241400-48243800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
8 | chr16:48241600-48244400 | Weak transcription | HepG2 | liver |
9 | chr16:48241800-48242600 | Enhancers | ES-WA7 Cell Line | embryonic stem cell |
10 | chr16:48241800-48244400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |