Variant report
Variant | rs11071396 |
---|---|
Chromosome Location | chr15:59051470-59051471 |
allele | A/C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr15:59049338..59052129-chr15:59052697..59054874,3 | K562 | blood: | |
2 | chr15:59042046..59047020-chr15:59050998..59056418,7 | K562 | blood: | |
3 | chr15:59051351..59055079-chr15:59061641..59063693,4 | K562 | blood: | |
4 | chr15:59040723..59043595-chr15:59050173..59052716,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000137845 | Chromatin interaction |
ENSG00000128923 | Chromatin interaction |
ENSG00000200318 | Chromatin interaction |
ENSG00000245975 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10851639 | 0.81[CHB][hapmap] |
rs11629654 | 0.80[EUR][1000 genomes] |
rs11852241 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11853043 | 0.88[YRI][hapmap] |
rs12437552 | 0.90[CHB][hapmap];0.90[AMR][1000 genomes] |
rs12439189 | 0.81[CHB][hapmap] |
rs1365772 | 0.81[CHB][hapmap] |
rs1427280 | 0.91[CHB][hapmap] |
rs17236243 | 0.91[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1869135 | 0.81[CHB][hapmap] |
rs2114573 | 0.91[CHB][hapmap] |
rs2414606 | 0.85[CHB][hapmap];0.90[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs2414607 | 0.85[CHB][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28391588 | 0.83[AMR][1000 genomes] |
rs28537903 | 0.82[EUR][1000 genomes] |
rs28617688 | 0.85[EUR][1000 genomes] |
rs34546804 | 0.87[EUR][1000 genomes] |
rs3764196 | 0.81[CHB][hapmap] |
rs3933541 | 0.90[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs394845 | 0.85[CHB][hapmap];0.90[ASN][1000 genomes] |
rs447299 | 0.80[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs4774309 | 0.91[CHB][hapmap] |
rs4774311 | 0.91[CEU][hapmap];0.89[EUR][1000 genomes] |
rs655348 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs681711 | 0.91[CEU][hapmap];0.95[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs694335 | 0.83[CEU][hapmap];0.95[CHB][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7164053 | 0.90[EUR][1000 genomes] |
rs7164844 | 0.90[CEU][hapmap];0.90[EUR][1000 genomes] |
rs7165259 | 0.81[CHB][hapmap] |
rs7168275 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7170538 | 0.90[CEU][hapmap];0.91[EUR][1000 genomes] |
rs7171198 | 0.91[CEU][hapmap];0.91[EUR][1000 genomes] |
rs7173286 | 0.86[CHB][hapmap];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7178970 | 0.87[EUR][1000 genomes] |
rs7179724 | 0.90[CHB][hapmap];0.85[AMR][1000 genomes] |
rs7182060 | 0.90[CHB][hapmap] |
rs7183504 | 0.84[AMR][1000 genomes] |
rs8023706 | 0.87[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs8027998 | 0.84[AMR][1000 genomes] |
rs8033478 | 0.90[EUR][1000 genomes] |
rs8036097 | 0.90[CHB][hapmap] |
rs9646204 | 0.90[CEU][hapmap];0.90[CHB][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs9744045 | 0.90[EUR][1000 genomes] |
rs9788674 | 0.88[CEU][hapmap];0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1051058 | chr15:58519922-59092530 | Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
2 | nsv542401 | chr15:58519922-59092530 | Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
3 | esv34110 | chr15:58949991-59381634 | Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 87 gene(s) | inside rSNPs | diseases |
4 | esv1843037 | chr15:59005922-59115159 | Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 37 gene(s) | inside rSNPs | diseases |
5 | esv1826703 | chr15:59005922-59213678 | Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 44 gene(s) | inside rSNPs | diseases |
6 | esv1798487 | chr15:59027139-59213678 | Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
7 | nsv428638 | chr15:59032300-59126567 | Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:59042600-59062600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr15:59043000-59062400 | Weak transcription | Psoas Muscle | Psoas |
3 | chr15:59047600-59052200 | Weak transcription | Fetal Thymus | thymus |