Variant report
Variant | rs16844689 |
---|---|
Chromosome Location | chr1:225521282-225521283 |
allele | C/T |
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] |
---|---|
rs10047221 | 1.00[CHB][hapmap];0.92[CHD][hapmap];0.89[JPT][hapmap];0.88[ASN][1000 genomes] |
rs10495236 | 1.00[CHB][hapmap];0.92[CHD][hapmap];0.84[JPT][hapmap];0.89[ASN][1000 genomes] |
rs10495238 | 1.00[CHB][hapmap];0.83[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes] |
rs10915814 | 0.88[ASN][1000 genomes] |
rs11580348 | 1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes] |
rs11585543 | 0.95[ASN][1000 genomes] |
rs12408441 | 0.89[ASN][1000 genomes] |
rs12408521 | 0.91[CEU][hapmap] |
rs12734615 | 0.85[EUR][1000 genomes] |
rs12744508 | 0.84[ASN][1000 genomes] |
rs12754197 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12759119 | 0.88[CEU][hapmap];0.83[MKK][hapmap] |
rs1480101 | 0.91[CEU][hapmap] |
rs1553447 | 0.88[CEU][hapmap];0.83[TSI][hapmap] |
rs16844602 | 0.88[CEU][hapmap] |
rs16844752 | 1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes] |
rs16844770 | 1.00[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes] |
rs16844772 | 1.00[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes] |
rs1842332 | 0.88[CEU][hapmap] |
rs34809641 | 0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs35833434 | 0.85[EUR][1000 genomes] |
rs4459070 | 0.80[ASN][1000 genomes] |
rs4539098 | 0.89[ASN][1000 genomes] |
rs4653418 | 1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes] |
rs4653420 | 1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[JPT][hapmap] |
rs4653628 | 0.88[CEU][hapmap];0.83[TSI][hapmap] |
rs55794003 | 0.85[EUR][1000 genomes] |
rs581675 | 0.88[CEU][hapmap] |
rs583098 | 0.88[CEU][hapmap] |
rs58840178 | 0.88[ASN][1000 genomes] |
rs60228869 | 0.92[ASN][1000 genomes] |
rs61850032 | 0.86[ASN][1000 genomes] |
rs638672 | 0.88[CEU][hapmap] |
rs6686051 | 0.89[ASN][1000 genomes] |
rs672951 | 0.88[CEU][hapmap] |
rs674025 | 0.91[CEU][hapmap] |
rs686493 | 0.91[CEU][hapmap] |
rs7523005 | 0.87[ASN][1000 genomes] |
rs7536245 | 0.91[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv945672 | chr1:225339532-225561349 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv873226 | chr1:225347689-225555602 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | esv1805729 | chr1:225404951-225526778 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | esv2757774 | chr1:225404951-225526778 | Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | esv2759002 | chr1:225404951-225526778 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv428312 | chr1:225404951-225526778 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | esv3370511 | chr1:225520629-225525227 | ZNF genes & repeats Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:225507200-225522800 | Weak transcription | Fetal Kidney | kidney |