Variant report
Variant | rs2014196 |
---|---|
Chromosome Location | chr7:21852615-21852616 |
allele | A/G |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10156026 | 0.86[JPT][hapmap] |
rs10227372 | 0.90[JPT][hapmap] |
rs10268039 | 0.90[JPT][hapmap] |
rs10268330 | 0.90[JPT][hapmap] |
rs11980396 | 0.90[JPT][hapmap] |
rs11983051 | 0.80[JPT][hapmap] |
rs12164106 | 0.90[JPT][hapmap] |
rs1541357 | 0.82[JPT][hapmap] |
rs1557778 | 0.90[JPT][hapmap] |
rs17145316 | 0.80[JPT][hapmap] |
rs2158128 | 0.90[JPT][hapmap] |
rs2285684 | 0.90[JPT][hapmap] |
rs2390592 | 0.81[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs2390593 | 0.82[ASN][1000 genomes] |
rs2893049 | 0.89[ASW][hapmap];0.89[CEU][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2893058 | 0.82[ASN][1000 genomes] |
rs3735523 | 0.96[CEU][hapmap];0.89[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4273751 | 0.90[JPT][hapmap] |
rs4722054 | 0.90[JPT][hapmap] |
rs6461598 | 0.90[JPT][hapmap] |
rs6946591 | 0.84[CEU][hapmap] |
rs6979777 | 0.90[JPT][hapmap] |
rs763543 | 0.90[JPT][hapmap] |
rs7777804 | 0.90[JPT][hapmap] |
rs7791639 | 0.90[JPT][hapmap] |
rs7806574 | 0.90[JPT][hapmap] |
rs961526 | 0.90[JPT][hapmap] |
rs979669 | 0.90[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1018133 | chr7:21740118-22055283 | Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv830922 | chr7:21793386-21964675 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
3 | nsv933320 | chr7:21840543-21882825 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |