Variant report
Variant | rs36199445 |
---|---|
Chromosome Location | chr7:16417931-16417932 |
allele | C/T |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:16406566..16408387-chr7:16416040..16418438,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10232515 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10240752 | 0.84[AMR][1000 genomes] |
rs10253784 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10259225 | 0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10267886 | 0.82[AMR][1000 genomes] |
rs10272029 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10950618 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12397698 | 0.80[AMR][1000 genomes] |
rs13234570 | 0.83[ASN][1000 genomes] |
rs17169465 | 0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2178597 | 0.82[AMR][1000 genomes] |
rs2389634 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs2389635 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs3903222 | 0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4351322 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs60155393 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6461248 | 0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6461250 | 0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6461251 | 0.80[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs6461252 | 0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6461254 | 0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6944820 | 0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6949292 | 0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6949353 | 0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6966496 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6976548 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7782304 | 0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7783283 | 0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7810822 | 0.86[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7811104 | 0.83[AMR][1000 genomes] |
rs9886352 | 0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1016642 | chr7:15884061-16799788 | Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription 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 | 56 gene(s) | inside rSNPs | diseases |
2 | esv2759514 | chr7:16236162-16527390 | Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
3 | nsv1022388 | chr7:16251992-16431864 | Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | esv2758105 | chr7:16272822-16527390 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
5 | esv2757215 | chr7:16346139-16458474 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
6 | nsv508447 | chr7:16360614-16446053 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1031019 | chr7:16377519-16458474 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers | Chromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
8 | nsv1028556 | chr7:16404615-16440024 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
9 | nsv523408 | chr7:16413481-16438357 | Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Strong transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
10 | nsv1034151 | chr7:16415497-16578081 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 11 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:16410800-16418200 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr7:16412600-16427000 | Weak transcription | Adipose Nuclei | Adipose |
3 | chr7:16414400-16425400 | Weak transcription | Aorta | Aorta |
4 | chr7:16415600-16423400 | Weak transcription | Ovary | ovary |
5 | chr7:16417600-16436800 | Weak transcription | Right Ventricle | heart |