Variant report
Variant | rs6902604 |
---|---|
Chromosome Location | chr6:49354537-49354538 |
allele | G/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] |
---|---|
rs10948498 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11752340 | 0.82[EUR][1000 genomes] |
rs11752910 | 0.82[EUR][1000 genomes] |
rs11755646 | 0.82[EUR][1000 genomes] |
rs11757098 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12173703 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12175251 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs16879241 | 0.86[EUR][1000 genomes] |
rs17805348 | 1.00[CEU][hapmap];0.94[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1924982 | 0.86[EUR][1000 genomes] |
rs2143730 | 0.82[EUR][1000 genomes] |
rs28841337 | 0.85[EUR][1000 genomes] |
rs471220 | 0.86[EUR][1000 genomes] |
rs471316 | 0.85[EUR][1000 genomes] |
rs471332 | 0.86[EUR][1000 genomes] |
rs472313 | 0.83[EUR][1000 genomes] |
rs474021 | 0.82[EUR][1000 genomes] |
rs474897 | 0.83[EUR][1000 genomes] |
rs475757 | 0.86[EUR][1000 genomes] |
rs478550 | 0.86[EUR][1000 genomes] |
rs481270 | 0.86[EUR][1000 genomes] |
rs481959 | 0.81[EUR][1000 genomes] |
rs482582 | 0.85[EUR][1000 genomes] |
rs482930 | 0.84[EUR][1000 genomes] |
rs483192 | 0.86[EUR][1000 genomes] |
rs483827 | 0.81[EUR][1000 genomes] |
rs484942 | 0.86[EUR][1000 genomes] |
rs485383 | 0.86[EUR][1000 genomes] |
rs485474 | 0.86[EUR][1000 genomes] |
rs485772 | 0.86[EUR][1000 genomes] |
rs485976 | 0.86[EUR][1000 genomes] |
rs495303 | 0.86[EUR][1000 genomes] |
rs495525 | 0.82[EUR][1000 genomes] |
rs496864 | 0.86[EUR][1000 genomes] |
rs498825 | 0.86[EUR][1000 genomes] |
rs500811 | 0.84[EUR][1000 genomes] |
rs501835 | 0.86[EUR][1000 genomes] |
rs503680 | 0.86[EUR][1000 genomes] |
rs512497 | 0.86[EUR][1000 genomes] |
rs520470 | 0.86[EUR][1000 genomes] |
rs520599 | 0.86[EUR][1000 genomes] |
rs527399 | 0.84[EUR][1000 genomes] |
rs529464 | 0.85[EUR][1000 genomes] |
rs530156 | 0.85[EUR][1000 genomes] |
rs530458 | 0.86[EUR][1000 genomes] |
rs532017 | 0.86[EUR][1000 genomes] |
rs532756 | 0.84[EUR][1000 genomes] |
rs532785 | 0.86[EUR][1000 genomes] |
rs537190 | 0.86[EUR][1000 genomes] |
rs538016 | 0.86[EUR][1000 genomes] |
rs539026 | 0.86[EUR][1000 genomes] |
rs540164 | 0.86[EUR][1000 genomes] |
rs543305 | 0.83[EUR][1000 genomes] |
rs543805 | 0.84[EUR][1000 genomes] |
rs544542 | 0.84[EUR][1000 genomes] |
rs545472 | 0.86[EUR][1000 genomes] |
rs547757 | 0.86[EUR][1000 genomes] |
rs548644 | 0.86[EUR][1000 genomes] |
rs549464 | 0.86[EUR][1000 genomes] |
rs551459 | 0.83[EUR][1000 genomes] |
rs551476 | 0.81[EUR][1000 genomes] |
rs553437 | 0.86[EUR][1000 genomes] |
rs555134 | 0.84[EUR][1000 genomes] |
rs556711 | 0.86[EUR][1000 genomes] |
rs556807 | 0.86[EUR][1000 genomes] |
rs559277 | 0.81[EUR][1000 genomes] |
rs562369 | 0.86[EUR][1000 genomes] |
rs563271 | 0.84[EUR][1000 genomes] |
rs563358 | 0.82[EUR][1000 genomes] |
rs564042 | 0.86[EUR][1000 genomes] |
rs568369 | 0.86[EUR][1000 genomes] |
rs568563 | 0.86[EUR][1000 genomes] |
rs569142 | 0.86[EUR][1000 genomes] |
rs574909 | 0.81[EUR][1000 genomes] |
rs575461 | 0.86[EUR][1000 genomes] |
rs577530 | 0.86[EUR][1000 genomes] |
rs579712 | 0.84[EUR][1000 genomes] |
rs580792 | 0.81[EUR][1000 genomes] |
rs6458682 | 0.82[EUR][1000 genomes] |
rs6902615 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6903158 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6922862 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6923065 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6927463 | 0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6935826 | 0.83[EUR][1000 genomes] |
rs72869253 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72870365 | 0.86[EUR][1000 genomes] |
rs7450140 | 0.84[EUR][1000 genomes] |
rs7764755 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9349492 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs9357609 | 0.82[EUR][1000 genomes] |
rs9357610 | 0.86[EUR][1000 genomes] |
rs9357612 | 0.84[EUR][1000 genomes] |
rs9367355 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9369883 | 0.81[EUR][1000 genomes] |
rs9369884 | 0.84[EUR][1000 genomes] |
rs9369886 | 0.86[EUR][1000 genomes] |
rs9369902 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9381766 | 0.84[EUR][1000 genomes] |
rs9381767 | 0.86[EUR][1000 genomes] |
rs9395477 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1024959 | chr6:49290141-49652124 | Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv1021136 | chr6:49295037-49631278 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
3 | nsv915806 | chr6:49313295-49430422 | Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
4 | nsv462943 | chr6:49319025-49376924 | Weak transcription Enhancers Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv603080 | chr6:49319025-49376924 | Enhancers Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:49354200-49355000 | Active TSS | K562 | blood |