Variant report
Variant | rs3128411 |
---|---|
Chromosome Location | chr7:112196223-112196224 |
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 | chr7:112188001..112190741-chr7:112193794..112196488,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12665935 | 0.87[ASN][1000 genomes] |
rs13232491 | 0.87[ASN][1000 genomes] |
rs1859882 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1971656 | 0.92[ASN][1000 genomes] |
rs2906789 | 0.96[CEU][hapmap] |
rs2966475 | 1.00[CEU][hapmap] |
rs3095042 | 0.96[CEU][hapmap];0.90[CHB][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs3095044 | 0.84[EUR][1000 genomes] |
rs3095045 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs3095046 | 0.86[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs3095047 | 0.80[EUR][1000 genomes] |
rs3095048 | 0.81[EUR][1000 genomes] |
rs3095049 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs3095051 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs3095053 | 0.83[EUR][1000 genomes] |
rs3095054 | 0.85[EUR][1000 genomes] |
rs3095057 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs3111448 | 0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3111451 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3111452 | 0.91[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs3111458 | 0.92[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs3111459 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs3128399 | 0.84[EUR][1000 genomes] |
rs3128413 | 0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs3128414 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs3128415 | 0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs3128420 | 0.88[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs3128422 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs3128423 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs3128424 | 1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs3128425 | 0.95[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs3128426 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs725312 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs978541 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531436 | chr7:111856171-112585407 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 105 gene(s) | inside rSNPs | diseases |
2 | esv1801382 | chr7:112167436-112205264 | Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv889055 | chr7:112174089-112353440 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | nsv971209 | chr7:112189312-112201673 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:112196200-112196800 | Enhancers | HMEC | breast |
2 | chr7:112196200-112197000 | Enhancers | Primary T cells from cord blood | blood |
3 | chr7:112196200-112197000 | Enhancers | Primary T helper cells PMA-I stimulated | -- |