Variant report
Variant | rs9375460 |
---|---|
Chromosome Location | chr6:127149538-127149539 |
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] |
---|---|
rs1077890 | 0.96[ASN][1000 genomes] |
rs1105955 | 0.89[ASN][1000 genomes] |
rs1105956 | 0.89[ASN][1000 genomes] |
rs11154369 | 0.80[ASN][1000 genomes] |
rs11154374 | 0.85[ASN][1000 genomes] |
rs11154375 | 0.86[ASN][1000 genomes] |
rs11154376 | 0.86[ASN][1000 genomes] |
rs11154377 | 0.86[ASN][1000 genomes] |
rs11154378 | 0.86[ASN][1000 genomes] |
rs11752270 | 0.92[ASN][1000 genomes] |
rs11752287 | 0.89[ASN][1000 genomes] |
rs11754167 | 0.85[ASN][1000 genomes] |
rs11754682 | 0.92[ASN][1000 genomes] |
rs11755390 | 0.88[ASN][1000 genomes] |
rs11756347 | 0.85[ASN][1000 genomes] |
rs11757951 | 0.83[ASN][1000 genomes] |
rs11759735 | 0.85[ASN][1000 genomes] |
rs12173960 | 0.89[ASN][1000 genomes] |
rs12234117 | 0.86[ASN][1000 genomes] |
rs12234163 | 0.86[ASN][1000 genomes] |
rs12664316 | 0.86[ASN][1000 genomes] |
rs13190766 | 0.92[ASN][1000 genomes] |
rs13196855 | 0.87[ASN][1000 genomes] |
rs13201060 | 0.93[ASN][1000 genomes] |
rs13201789 | 0.96[ASN][1000 genomes] |
rs13204751 | 0.86[ASN][1000 genomes] |
rs13207064 | 0.92[ASN][1000 genomes] |
rs13207638 | 0.91[ASN][1000 genomes] |
rs13209747 | 0.85[ASN][1000 genomes] |
rs13213649 | 0.86[ASN][1000 genomes] |
rs13215166 | 0.93[ASN][1000 genomes] |
rs13216524 | 0.96[ASN][1000 genomes] |
rs1361831 | 0.88[ASN][1000 genomes] |
rs1539554 | 0.96[ASN][1000 genomes] |
rs1539556 | 0.96[ASN][1000 genomes] |
rs1543705 | 0.88[ASN][1000 genomes] |
rs1543706 | 0.88[ASN][1000 genomes] |
rs1543707 | 0.88[ASN][1000 genomes] |
rs1592287 | 0.86[ASN][1000 genomes] |
rs1592288 | 0.86[ASN][1000 genomes] |
rs17570053 | 0.91[ASN][1000 genomes] |
rs1832986 | 0.88[ASN][1000 genomes] |
rs1930942 | 0.88[ASN][1000 genomes] |
rs1930943 | 0.88[ASN][1000 genomes] |
rs1930944 | 0.88[ASN][1000 genomes] |
rs2021707 | 0.85[ASN][1000 genomes] |
rs2021708 | 0.85[ASN][1000 genomes] |
rs2022477 | 0.85[ASN][1000 genomes] |
rs2022478 | 0.85[ASN][1000 genomes] |
rs2022479 | 0.85[ASN][1000 genomes] |
rs2077111 | 0.89[ASN][1000 genomes] |
rs2143679 | 0.85[ASN][1000 genomes] |
rs2179723 | 0.85[ASN][1000 genomes] |
rs3195537 | 0.86[ASN][1000 genomes] |
rs34072374 | 0.88[ASN][1000 genomes] |
rs34259221 | 0.85[ASN][1000 genomes] |
rs34443655 | 0.92[ASN][1000 genomes] |
rs34656055 | 0.93[ASN][1000 genomes] |
rs34937037 | 0.83[ASN][1000 genomes] |
rs35108222 | 0.86[ASN][1000 genomes] |
rs35111006 | 0.85[ASN][1000 genomes] |
rs35211576 | 0.85[ASN][1000 genomes] |
rs35697500 | 0.86[ASN][1000 genomes] |
rs35870379 | 0.88[ASN][1000 genomes] |
rs35900147 | 0.93[ASN][1000 genomes] |
rs3926855 | 0.88[ASN][1000 genomes] |
rs4424110 | 0.86[ASN][1000 genomes] |
rs4618551 | 0.86[ASN][1000 genomes] |
rs4897190 | 0.88[ASN][1000 genomes] |
rs58274947 | 0.86[ASN][1000 genomes] |
rs59540076 | 0.92[ASN][1000 genomes] |
rs62426305 | 0.81[ASN][1000 genomes] |
rs62426327 | 0.96[ASN][1000 genomes] |
rs62436813 | 0.84[ASN][1000 genomes] |
rs62439171 | 0.86[ASN][1000 genomes] |
rs62439174 | 0.86[ASN][1000 genomes] |
rs62439175 | 0.86[ASN][1000 genomes] |
rs62439176 | 0.86[ASN][1000 genomes] |
rs6902861 | 0.88[ASN][1000 genomes] |
rs6908014 | 0.96[ASN][1000 genomes] |
rs6920370 | 0.88[ASN][1000 genomes] |
rs6921132 | 0.88[ASN][1000 genomes] |
rs6940295 | 0.88[ASN][1000 genomes] |
rs6940442 | 0.83[ASN][1000 genomes] |
rs6941106 | 0.88[ASN][1000 genomes] |
rs761356 | 0.89[ASN][1000 genomes] |
rs7739746 | 0.85[ASN][1000 genomes] |
rs7745882 | 0.88[ASN][1000 genomes] |
rs7746534 | 0.88[ASN][1000 genomes] |
rs7753502 | 0.86[ASN][1000 genomes] |
rs7758037 | 0.86[ASN][1000 genomes] |
rs7766269 | 0.88[ASN][1000 genomes] |
rs9372844 | 0.88[ASN][1000 genomes] |
rs9372845 | 0.96[ASN][1000 genomes] |
rs9372849 | 0.88[ASN][1000 genomes] |
rs9372850 | 0.86[ASN][1000 genomes] |
rs9372851 | 0.81[ASN][1000 genomes] |
rs9375454 | 0.85[ASN][1000 genomes] |
rs9375455 | 0.85[ASN][1000 genomes] |
rs9375456 | 0.86[ASN][1000 genomes] |
rs9375457 | 0.88[ASN][1000 genomes] |
rs9375459 | 0.96[ASN][1000 genomes] |
rs9375472 | 0.93[ASN][1000 genomes] |
rs9375474 | 0.92[ASN][1000 genomes] |
rs9375477 | 0.83[ASN][1000 genomes] |
rs9385405 | 0.83[ASN][1000 genomes] |
rs9385410 | 0.88[ASN][1000 genomes] |
rs9388519 | 0.85[ASN][1000 genomes] |
rs9388520 | 0.85[ASN][1000 genomes] |
rs9388521 | 0.86[ASN][1000 genomes] |
rs9388522 | 0.86[ASN][1000 genomes] |
rs9388523 | 0.86[ASN][1000 genomes] |
rs9388524 | 0.86[ASN][1000 genomes] |
rs9388525 | 0.89[ASN][1000 genomes] |
rs9388530 | 0.96[ASN][1000 genomes] |
rs9388535 | 0.93[ASN][1000 genomes] |
rs9388537 | 0.88[ASN][1000 genomes] |
rs9398816 | 0.83[ASN][1000 genomes] |
rs9398817 | 0.85[ASN][1000 genomes] |
rs9398821 | 0.93[ASN][1000 genomes] |
rs9398822 | 0.92[ASN][1000 genomes] |
rs9398823 | 0.88[ASN][1000 genomes] |
rs9401908 | 0.83[ASN][1000 genomes] |
rs9401912 | 0.96[ASN][1000 genomes] |
rs983668 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1026498 | chr6:126812609-127397240 | Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv1024206 | chr6:126873187-127475713 | Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv538438 | chr6:126873187-127475713 | Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv1020322 | chr6:127087551-127331285 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:127146600-127149600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr6:127147800-127152000 | Weak transcription | HUVEC | blood vessel |