Variant report
Variant | rs12192587 |
---|---|
Chromosome Location | chr6:74673330-74673331 |
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 |
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No data |
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No data |
rs_ID | r2[population] |
---|---|
rs12190633 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12191694 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs12196321 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12207763 | 0.91[EUR][1000 genomes] |
rs12208415 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs12211362 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs12211795 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs12212963 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs12213134 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12213921 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs55646316 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs55674204 | 1.00[ASN][1000 genomes] |
rs72949471 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs72952354 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs72953230 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72953279 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs72955120 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs72955121 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs72955125 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs72955129 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs72955133 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs72955136 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs72955140 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs72961296 | 1.00[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs72965241 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv463154 | chr6:74412048-74775904 | Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv603695 | chr6:74412048-74775904 | Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
3 | esv34305 | chr6:74571797-74675280 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv1030389 | chr6:74606701-74811706 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv3394316 | chr6:74630005-74935625 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1019469 | chr6:74644208-74702416 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv603733 | chr6:74666559-74944460 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:74672800-74673400 | Enhancers | HUES64 Cell Line | embryonic stem cell |
2 | chr6:74673200-74674000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |