Variant report
Variant | rs7114742 |
---|---|
Chromosome Location | chr11:16082343-16082344 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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rs_ID | r2[population] |
---|---|
rs10500821 | 1.00[TSI][hapmap] |
rs10500822 | 1.00[TSI][hapmap] |
rs10500825 | 1.00[TSI][hapmap] |
rs1074953 | 1.00[EUR][1000 genomes] |
rs11023752 | 1.00[EUR][1000 genomes] |
rs12099171 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12574859 | 1.00[TSI][hapmap] |
rs12574862 | 1.00[TSI][hapmap] |
rs12577378 | 1.00[TSI][hapmap] |
rs12577495 | 1.00[TSI][hapmap] |
rs1455101 | 1.00[TSI][hapmap] |
rs16932405 | 1.00[TSI][hapmap] |
rs16932409 | 1.00[TSI][hapmap] |
rs16932416 | 1.00[TSI][hapmap] |
rs16932455 | 1.00[TSI][hapmap] |
rs16932458 | 1.00[TSI][hapmap] |
rs16932474 | 0.89[ASW][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs16932477 | 0.82[YRI][hapmap];1.00[EUR][1000 genomes] |
rs16932507 | 0.82[YRI][hapmap];1.00[EUR][1000 genomes] |
rs16932558 | 1.00[EUR][1000 genomes] |
rs16932580 | 1.00[TSI][hapmap] |
rs16932585 | 1.00[TSI][hapmap] |
rs16932620 | 1.00[TSI][hapmap] |
rs4279976 | 1.00[TSI][hapmap] |
rs4478958 | 1.00[TSI][hapmap] |
rs55776402 | 1.00[EUR][1000 genomes] |
rs55797092 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55836990 | 1.00[EUR][1000 genomes] |
rs56003030 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56013327 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56039367 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56077417 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56110890 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56214661 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56336701 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56339948 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56395489 | 1.00[EUR][1000 genomes] |
rs56710873 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57058857 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57059428 | 1.00[EUR][1000 genomes] |
rs57534454 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57594599 | 1.00[EUR][1000 genomes] |
rs58248240 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58385655 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58476737 | 1.00[EUR][1000 genomes] |
rs59156755 | 1.00[EUR][1000 genomes] |
rs59237138 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59275453 | 1.00[EUR][1000 genomes] |
rs59355840 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59732810 | 1.00[EUR][1000 genomes] |
rs59749270 | 1.00[EUR][1000 genomes] |
rs60041887 | 1.00[EUR][1000 genomes] |
rs60082792 | 1.00[EUR][1000 genomes] |
rs60488672 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60693734 | 1.00[EUR][1000 genomes] |
rs60695570 | 1.00[EUR][1000 genomes] |
rs60855295 | 1.00[EUR][1000 genomes] |
rs60900176 | 1.00[EUR][1000 genomes] |
rs60968744 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61000891 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61145028 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61292713 | 1.00[EUR][1000 genomes] |
rs61560681 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61573169 | 1.00[EUR][1000 genomes] |
rs6486273 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7101975 | 1.00[EUR][1000 genomes] |
rs7103044 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7103298 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7105445 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7118842 | 1.00[EUR][1000 genomes] |
rs7120852 | 1.00[EUR][1000 genomes] |
rs7122351 | 0.84[LWK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7126907 | 1.00[EUR][1000 genomes] |
rs7128209 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7128216 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7128226 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7128933 | 1.00[EUR][1000 genomes] |
rs7130519 | 1.00[EUR][1000 genomes] |
rs7130995 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73417010 | 1.00[EUR][1000 genomes] |
rs73417011 | 1.00[EUR][1000 genomes] |
rs73417012 | 1.00[EUR][1000 genomes] |
rs73417015 | 1.00[EUR][1000 genomes] |
rs7926258 | 1.00[EUR][1000 genomes] |
rs7933131 | 0.84[LWK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7936618 | 0.95[LWK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7942659 | 1.00[TSI][hapmap] |
rs7949999 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs894006 | 1.00[EUR][1000 genomes] |
rs9666192 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9667689 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832074 | chr11:15927105-16100772 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16024800-16088200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr11:16043000-16102000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr11:16065600-16085400 | Weak transcription | Fetal Heart | heart |
4 | chr11:16068800-16103800 | Weak transcription | Left Ventricle | heart |
5 | chr11:16074800-16082800 | Weak transcription | Fetal Intestine Large | intestine |
6 | chr11:16074800-16092200 | Weak transcription | Fetal Intestine Small | intestine |
7 | chr11:16075200-16092600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
8 | chr11:16078000-16083000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
9 | chr11:16079600-16086400 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
10 | chr11:16081000-16084000 | Weak transcription | Skeletal Muscle Male | skeletal muscle |