Variant report
Variant | rs12200908 |
---|---|
Chromosome Location | chr6:73440384-73440385 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:73438791..73440476-chr6:73442426..73445247,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10455268 | 1.00[CHB][hapmap] |
rs10484913 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10485213 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10943048 | 1.00[ASN][1000 genomes] |
rs10943050 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10943051 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10943055 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10943057 | 1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10943058 | 1.00[ASN][1000 genomes] |
rs11759937 | 0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs12189933 | 1.00[CHB][hapmap] |
rs12189974 | 1.00[ASN][1000 genomes] |
rs12191039 | 1.00[ASN][1000 genomes] |
rs12191216 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs12191848 | 1.00[ASN][1000 genomes] |
rs12192751 | 0.90[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12194741 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12195259 | 1.00[ASN][1000 genomes] |
rs12197962 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12199549 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12200468 | 1.00[CHB][hapmap] |
rs12201380 | 1.00[ASN][1000 genomes] |
rs12204139 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12204989 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs12205374 | 1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12208053 | 1.00[CHB][hapmap] |
rs12208907 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12210850 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12211580 | 1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12212268 | 1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12212419 | 1.00[ASN][1000 genomes] |
rs12212562 | 1.00[CHB][hapmap] |
rs12212818 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12214894 | 1.00[CHB][hapmap] |
rs12214895 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12215865 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12374630 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12374631 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs17692715 | 1.00[CHB][hapmap] |
rs17692874 | 1.00[CHB][hapmap] |
rs17692898 | 1.00[CHB][hapmap] |
rs17729195 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17749408 | 1.00[CHB][hapmap] |
rs17749420 | 1.00[CHB][hapmap] |
rs17796704 | 1.00[ASN][1000 genomes] |
rs1928153 | 1.00[ASN][1000 genomes] |
rs62411986 | 1.00[ASN][1000 genomes] |
rs62411990 | 1.00[ASN][1000 genomes] |
rs6453591 | 1.00[CHB][hapmap] |
rs6931918 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6935174 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs719830 | 1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs72935423 | 0.84[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73753888 | 0.85[EUR][1000 genomes] |
rs7748594 | 1.00[ASN][1000 genomes] |
rs7768673 | 1.00[CHB][hapmap] |
rs7772197 | 0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7776215 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023809 | chr6:73157813-73477997 | Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv538303 | chr6:73157813-73477997 | Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | esv3347486 | chr6:73283590-73445976 | Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv830689 | chr6:73385557-73544404 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv830690 | chr6:73391428-73574304 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv970046 | chr6:73438631-73444293 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:73437800-73441800 | Weak transcription | Primary B cells from peripheral blood | blood |
2 | chr6:73437800-73455200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr6:73438400-73455400 | Weak transcription | HMEC | breast |
4 | chr6:73438600-73440800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr6:73438600-73443000 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
6 | chr6:73438600-73447800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
7 | chr6:73439800-73441800 | Weak transcription | Psoas Muscle | Psoas |