Variant report
Variant | rs11723877 |
---|---|
Chromosome Location | chr4:119130671-119130672 |
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] |
---|---|
rs10001926 | 0.87[ASN][1000 genomes] |
rs10002634 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10008013 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10014055 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10014957 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10016206 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10016301 | 0.97[ASN][1000 genomes] |
rs10018844 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10024837 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10025690 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10033927 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10213280 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1028091 | 0.80[ASN][1000 genomes] |
rs1045817 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11721634 | 0.80[ASN][1000 genomes] |
rs11723996 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11726746 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11726838 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11727684 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11727817 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11728941 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11730327 | 0.80[ASN][1000 genomes] |
rs11730687 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11731179 | 0.93[ASN][1000 genomes] |
rs11734145 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11930782 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11933280 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11934183 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11944227 | 1.00[ASN][1000 genomes] |
rs11945329 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11945537 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11945882 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11947244 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11947630 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13114867 | 0.97[ASN][1000 genomes] |
rs13129847 | 0.97[ASN][1000 genomes] |
rs13435006 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1403845 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1403846 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1523744 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1523745 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1523746 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1589718 | 0.97[ASN][1000 genomes] |
rs17515832 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17516430 | 0.80[ASN][1000 genomes] |
rs17594054 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17594243 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1996725 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2030633 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2030634 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2204269 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2271577 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2271578 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2272160 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28396217 | 1.00[ASN][1000 genomes] |
rs28508556 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28661939 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs3817274 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4546315 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56007507 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56258393 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56305917 | 0.80[ASN][1000 genomes] |
rs56339949 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56390335 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs57605165 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58798110 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60858456 | 0.93[ASN][1000 genomes] |
rs61342457 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61443542 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62326151 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6534088 | 0.93[ASN][1000 genomes] |
rs6822408 | 0.93[ASN][1000 genomes] |
rs6822996 | 1.00[ASN][1000 genomes] |
rs6842372 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6842689 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6853879 | 0.97[ASN][1000 genomes] |
rs6855052 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6855536 | 0.90[ASN][1000 genomes] |
rs6856076 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71608347 | 0.97[ASN][1000 genomes] |
rs71608349 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72907147 | 0.93[ASN][1000 genomes] |
rs72907175 | 0.93[ASN][1000 genomes] |
rs72909175 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72909186 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72917104 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72917146 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72917175 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72917179 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7661522 | 0.97[ASN][1000 genomes] |
rs7685455 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9992827 | 0.97[ASN][1000 genomes] |
rs9996753 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9996762 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv519017 | chr4:118828807-119771481 | Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
2 | nsv1009076 | chr4:118949490-119269424 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | nsv1001236 | chr4:118949490-119271243 | Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
4 | nsv1008236 | chr4:118989467-119154024 | ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv999152 | chr4:119001143-119138322 | Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | esv34038 | chr4:119035124-119455391 | Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
7 | nsv1001138 | chr4:119095147-119461837 | Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
8 | nsv537230 | chr4:119095147-119461837 | Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
9 | nsv4485 | chr4:119103349-119144334 | Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
10 | esv3524414 | chr4:119106398-119131703 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding region | 1 gene(s) | inside rSNPs | n/a |
11 | esv3524415 | chr4:119106398-119131703 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS | TF binding region | 1 gene(s) | inside rSNPs | n/a |
12 | nsv511250 | chr4:119115366-119134308 | Enhancers ZNF genes & repeats Weak transcription Strong transcription | TF binding region | 1 gene(s) | inside rSNPs | n/a |
13 | nsv966561 | chr4:119115482-119130733 | Enhancers ZNF genes & repeats Weak transcription Strong transcription | TF binding region | 1 gene(s) | inside rSNPs | n/a |
14 | esv3466068 | chr4:119123504-119132102 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | n/a | n/a | inside rSNPs | n/a |
15 | esv3529961 | chr4:119124154-119131352 | Enhancers Weak transcription ZNF genes & repeats Strong transcription | n/a | n/a | inside rSNPs | n/a |
16 | esv3529958 | chr4:119124654-119131252 | Enhancers ZNF genes & repeats Strong transcription Weak transcription | n/a | n/a | inside rSNPs | n/a |
17 | nsv1002771 | chr4:119125361-119571237 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
18 | nsv595300 | chr4:119126335-119134308 | Strong transcription Enhancers Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
19 | nsv595321 | chr4:119127398-119134308 | Enhancers Weak transcription Strong transcription | n/a | n/a | inside rSNPs | n/a |
20 | nsv595324 | chr4:119127445-119134308 | Enhancers Weak transcription Strong transcription | n/a | n/a | inside rSNPs | n/a |
21 | nsv595330 | chr4:119128463-119134308 | Weak transcription Enhancers Strong transcription | n/a | n/a | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:119127600-119131200 | Strong transcription | Dnd41 | blood |
2 | chr4:119129800-119130800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
3 | chr4:119130400-119131400 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
4 | chr4:119130400-119131600 | Enhancers | HUES6 Cell Line | embryonic stem cell |
5 | chr4:119130600-119130800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
6 | chr4:119130600-119131200 | Enhancers | HUES64 Cell Line | embryonic stem cell |
7 | chr4:119130600-119131400 | Enhancers | HUES48 Cell Line | embryonic stem cell |