Variant report
Variant | rs1387419 |
---|---|
Chromosome Location | chr6:74977604-74977605 |
allele | A/C |
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] |
---|---|
rs1038684 | 0.92[EUR][1000 genomes] |
rs10485385 | 0.92[EUR][1000 genomes] |
rs10485386 | 0.92[EUR][1000 genomes] |
rs10485387 | 0.92[EUR][1000 genomes] |
rs10805997 | 0.92[EUR][1000 genomes] |
rs12175094 | 0.92[EUR][1000 genomes] |
rs12523779 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12524014 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12525068 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12527310 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12528947 | 0.92[EUR][1000 genomes] |
rs1387418 | 0.92[EUR][1000 genomes] |
rs1387420 | 0.92[EUR][1000 genomes] |
rs1416395 | 0.91[EUR][1000 genomes] |
rs1416396 | 0.91[EUR][1000 genomes] |
rs1416397 | 0.89[EUR][1000 genomes] |
rs1416398 | 0.92[EUR][1000 genomes] |
rs1489380 | 0.92[EUR][1000 genomes] |
rs1552564 | 0.92[EUR][1000 genomes] |
rs1552565 | 0.91[EUR][1000 genomes] |
rs16884558 | 0.92[EUR][1000 genomes] |
rs16884590 | 0.92[EUR][1000 genomes] |
rs1844317 | 0.92[EUR][1000 genomes] |
rs1953176 | 0.92[EUR][1000 genomes] |
rs2029393 | 0.92[EUR][1000 genomes] |
rs2029394 | 0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2068742 | 0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2200809 | 0.92[EUR][1000 genomes] |
rs34261519 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4120421 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4706577 | 0.92[EUR][1000 genomes] |
rs4706578 | 0.92[EUR][1000 genomes] |
rs4708141 | 0.92[EUR][1000 genomes] |
rs4708142 | 0.92[EUR][1000 genomes] |
rs60997457 | 0.87[EUR][1000 genomes] |
rs67514214 | 0.87[EUR][1000 genomes] |
rs6907419 | 0.82[EUR][1000 genomes] |
rs72950553 | 0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs72953713 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72953738 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72953745 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72954310 | 0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72959610 | 0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72959903 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72964264 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs72964267 | 0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs72967270 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs73460274 | 0.87[EUR][1000 genomes] |
rs7746000 | 0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7752957 | 0.92[EUR][1000 genomes] |
rs7776197 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9293958 | 0.91[EUR][1000 genomes] |
rs9293959 | 0.92[EUR][1000 genomes] |
rs9293960 | 0.92[EUR][1000 genomes] |
rs9293962 | 0.92[EUR][1000 genomes] |
rs9293964 | 0.92[EUR][1000 genomes] |
rs9341460 | 0.91[EUR][1000 genomes] |
rs9341461 | 0.87[EUR][1000 genomes] |
rs9343123 | 0.92[EUR][1000 genomes] |
rs9343127 | 0.87[EUR][1000 genomes] |
rs9343128 | 0.87[EUR][1000 genomes] |
rs9343138 | 0.82[EUR][1000 genomes] |
rs9352083 | 0.92[EUR][1000 genomes] |
rs9352084 | 0.92[EUR][1000 genomes] |
rs9352085 | 0.92[EUR][1000 genomes] |
rs9352087 | 0.90[CEU][hapmap];0.93[TSI][hapmap];0.92[EUR][1000 genomes] |
rs9359076 | 0.92[EUR][1000 genomes] |
rs9360757 | 0.92[EUR][1000 genomes] |
rs9360759 | 0.92[EUR][1000 genomes] |
rs9360761 | 0.92[EUR][1000 genomes] |
rs9360763 | 0.92[EUR][1000 genomes] |
rs9360766 | 0.88[EUR][1000 genomes] |
rs9360769 | 0.87[EUR][1000 genomes] |
rs9360770 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv886162 | chr6:74903797-75006170 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv886163 | chr6:74944460-75006170 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
3 | nsv886164 | chr6:74944460-75024313 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | esv2758061 | chr6:74961996-75128165 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv2759442 | chr6:74961996-75162222 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | esv2829863 | chr6:74976178-75040446 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:74976800-74979000 | Weak transcription | Fetal Muscle Leg | muscle |