Variant report
Variant | rs11927016 |
---|---|
Chromosome Location | chr3:143125855-143125856 |
allele | A/G |
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 | chr3:142702091..142703863-chr3:143124368..143127193,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10446326 | 0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs10513200 | 0.83[CEU][hapmap] |
rs10513210 | 1.00[CHB][hapmap] |
rs10804692 | 1.00[CHB][hapmap] |
rs11708401 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs11711068 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11717437 | 1.00[CHB][hapmap] |
rs11718728 | 0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11915421 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11915761 | 0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs13061014 | 1.00[CHB][hapmap] |
rs13072761 | 0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs13074801 | 1.00[CHB][hapmap] |
rs13081068 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13099124 | 0.94[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1501631 | 1.00[CHB][hapmap] |
rs1604377 | 1.00[CHB][hapmap] |
rs1604380 | 1.00[CHB][hapmap] |
rs1609727 | 1.00[CHB][hapmap] |
rs1610217 | 1.00[CHB][hapmap] |
rs16853767 | 1.00[CHB][hapmap] |
rs16853866 | 1.00[CHB][hapmap] |
rs16853903 | 1.00[CHB][hapmap] |
rs17637392 | 1.00[CHB][hapmap] |
rs1808882 | 1.00[CHB][hapmap] |
rs1812200 | 1.00[CHB][hapmap] |
rs1846960 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1875462 | 1.00[CHB][hapmap] |
rs1995356 | 1.00[CHB][hapmap] |
rs2083528 | 1.00[CHB][hapmap] |
rs4024563 | 1.00[CHB][hapmap] |
rs4839627 | 1.00[CHB][hapmap] |
rs5003886 | 1.00[CHB][hapmap] |
rs67478180 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6784124 | 1.00[CHB][hapmap] |
rs7627844 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7642361 | 1.00[CHB][hapmap] |
rs7652557 | 0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs894176 | 1.00[CHB][hapmap] |
rs9850863 | 1.00[CHB][hapmap] |
rs9862119 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949288 | chr3:142793323-143585882 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
2 | esv2757894 | chr3:142992697-143285979 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
3 | esv2759184 | chr3:142992697-143285979 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv999000 | chr3:143086325-143136128 | Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:143100600-143142600 | Weak transcription | Primary T cells from cord blood | blood |
2 | chr3:143125800-143126600 | Enhancers | Dnd41 | blood |