Variant report
Variant | rs17139920 |
---|---|
Chromosome Location | chr7:117110081-117110082 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | 7:117100350-117112126..7:117341506-117356953 | GM12878 | blood: | |
2 | 7:117100350-117112126..7:117326534-117332210 | H1-hESC | embryonic stem cell: | embryo |
3 | 7:116580605-116585719..7:117100350-117112126 | H1-hESC | embryonic stem cell: | embryo |
4 | chr7:117107707..117110294-chr7:117111075..117113526,2 | MCF-7 | breast: | |
5 | chr7:117108067..117110269-chr7:117111131..117113767,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000222150 | Chromatin interaction |
ENSG00000001626 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10487371 | 0.80[YRI][hapmap] |
rs17139922 | 0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs17347210 | 0.80[YRI][hapmap];0.93[AMR][1000 genomes] |
rs4571678 | 0.87[YRI][hapmap] |
rs73717524 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs989727 | 0.83[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv889076 | chr7:117064625-117147547 | Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |