Variant report
Variant | rs9426165 |
---|---|
Chromosome Location | chr1:225178787-225178788 |
allele | A/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] |
---|---|
rs10495228 | 0.82[ASN][1000 genomes] |
rs10495229 | 0.86[ASN][1000 genomes] |
rs10495230 | 0.83[ASN][1000 genomes] |
rs12561993 | 0.85[ASN][1000 genomes] |
rs12562917 | 0.88[ASN][1000 genomes] |
rs12563033 | 0.85[ASN][1000 genomes] |
rs12563857 | 0.85[ASN][1000 genomes] |
rs12563866 | 0.88[ASN][1000 genomes] |
rs12564683 | 0.81[ASN][1000 genomes] |
rs12564768 | 0.88[ASN][1000 genomes] |
rs12564776 | 0.88[ASN][1000 genomes] |
rs12565019 | 0.82[ASN][1000 genomes] |
rs12565073 | 0.88[ASN][1000 genomes] |
rs12565439 | 0.86[ASN][1000 genomes] |
rs12565833 | 0.88[ASN][1000 genomes] |
rs12566396 | 0.86[ASN][1000 genomes] |
rs12566857 | 0.86[ASN][1000 genomes] |
rs12566886 | 0.86[ASN][1000 genomes] |
rs12567069 | 0.88[ASN][1000 genomes] |
rs12567461 | 0.82[ASN][1000 genomes] |
rs12567470 | 0.82[ASN][1000 genomes] |
rs12567499 | 0.86[ASN][1000 genomes] |
rs12567812 | 0.88[ASN][1000 genomes] |
rs12568142 | 0.85[ASN][1000 genomes] |
rs1482279 | 0.86[ASN][1000 genomes] |
rs1482280 | 0.83[ASN][1000 genomes] |
rs1506070 | 0.85[ASN][1000 genomes] |
rs1587980 | 0.85[ASN][1000 genomes] |
rs1600865 | 0.81[ASN][1000 genomes] |
rs16857787 | 0.82[ASN][1000 genomes] |
rs16858145 | 0.82[ASN][1000 genomes] |
rs16858216 | 0.82[ASN][1000 genomes] |
rs16858299 | 0.81[ASN][1000 genomes] |
rs16858661 | 0.86[ASN][1000 genomes] |
rs16858758 | 0.86[ASN][1000 genomes] |
rs16858766 | 0.86[ASN][1000 genomes] |
rs16858829 | 0.86[ASN][1000 genomes] |
rs16858831 | 0.86[ASN][1000 genomes] |
rs16858932 | 0.86[ASN][1000 genomes] |
rs16858962 | 0.86[ASN][1000 genomes] |
rs1905113 | 0.85[ASN][1000 genomes] |
rs1905114 | 0.86[ASN][1000 genomes] |
rs1905115 | 0.86[ASN][1000 genomes] |
rs1905117 | 0.86[ASN][1000 genomes] |
rs1936629 | 0.81[ASN][1000 genomes] |
rs1982707 | 0.86[ASN][1000 genomes] |
rs2101143 | 0.82[ASN][1000 genomes] |
rs2291227 | 0.86[ASN][1000 genomes] |
rs2406098 | 0.82[ASN][1000 genomes] |
rs2449257 | 0.88[ASN][1000 genomes] |
rs2449259 | 0.88[ASN][1000 genomes] |
rs2449260 | 0.88[ASN][1000 genomes] |
rs2449273 | 0.85[ASN][1000 genomes] |
rs2449274 | 0.85[ASN][1000 genomes] |
rs2449276 | 0.85[ASN][1000 genomes] |
rs2449280 | 0.85[ASN][1000 genomes] |
rs2449292 | 0.88[ASN][1000 genomes] |
rs2449311 | 0.85[ASN][1000 genomes] |
rs2449313 | 0.85[ASN][1000 genomes] |
rs2449316 | 0.82[ASN][1000 genomes] |
rs2456335 | 0.83[ASN][1000 genomes] |
rs2456339 | 0.85[ASN][1000 genomes] |
rs2456340 | 0.85[ASN][1000 genomes] |
rs2489300 | 0.86[ASN][1000 genomes] |
rs2489302 | 0.81[ASN][1000 genomes] |
rs2489310 | 0.81[ASN][1000 genomes] |
rs2489322 | 0.88[ASN][1000 genomes] |
rs2489328 | 0.88[ASN][1000 genomes] |
rs2489330 | 0.88[ASN][1000 genomes] |
rs2489332 | 0.83[ASN][1000 genomes] |
rs2489341 | 0.88[ASN][1000 genomes] |
rs2489344 | 0.88[ASN][1000 genomes] |
rs2501061 | 0.86[ASN][1000 genomes] |
rs2501064 | 0.86[ASN][1000 genomes] |
rs2501066 | 0.86[ASN][1000 genomes] |
rs2501081 | 0.82[ASN][1000 genomes] |
rs2501125 | 0.86[ASN][1000 genomes] |
rs2501127 | 0.83[ASN][1000 genomes] |
rs2501129 | 0.86[ASN][1000 genomes] |
rs2501130 | 0.88[ASN][1000 genomes] |
rs2501134 | 0.88[ASN][1000 genomes] |
rs2501135 | 0.84[ASN][1000 genomes] |
rs2501140 | 0.86[ASN][1000 genomes] |
rs2501141 | 0.86[ASN][1000 genomes] |
rs2501143 | 0.84[ASN][1000 genomes] |
rs2501153 | 0.86[ASN][1000 genomes] |
rs2501156 | 0.86[ASN][1000 genomes] |
rs4379650 | 0.82[ASN][1000 genomes] |
rs55668169 | 0.86[ASN][1000 genomes] |
rs55754430 | 0.82[ASN][1000 genomes] |
rs55761817 | 0.84[ASN][1000 genomes] |
rs55785201 | 0.83[ASN][1000 genomes] |
rs55786647 | 0.86[ASN][1000 genomes] |
rs55876129 | 0.85[ASN][1000 genomes] |
rs55962425 | 0.85[ASN][1000 genomes] |
rs56088704 | 0.86[ASN][1000 genomes] |
rs56152573 | 0.86[ASN][1000 genomes] |
rs56251723 | 0.83[ASN][1000 genomes] |
rs56337810 | 0.83[ASN][1000 genomes] |
rs57889280 | 0.83[ASN][1000 genomes] |
rs61466304 | 0.82[ASN][1000 genomes] |
rs6677680 | 0.82[ASN][1000 genomes] |
rs6697156 | 0.85[ASN][1000 genomes] |
rs729398 | 0.82[ASN][1000 genomes] |
rs7523949 | 0.86[ASN][1000 genomes] |
rs7531542 | 0.85[ASN][1000 genomes] |
rs981068 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2757773 | chr1:225087924-225253274 | Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | esv2759001 | chr1:225087924-225253274 | Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | esv3438976 | chr1:225133567-225248753 | Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv1804634 | chr1:225137134-225206826 | Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv873225 | chr1:225162060-225373936 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:225157600-225201400 | Weak transcription | Pancreas | Pancrea |