Variant report
Variant | rs10015087 |
---|---|
Chromosome Location | chr4:94337423-94337424 |
allele | G/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] |
---|---|
rs10002534 | 0.82[EUR][1000 genomes] |
rs10010189 | 0.81[EUR][1000 genomes] |
rs10010334 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10012194 | 0.94[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10012783 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10019267 | 1.00[ASN][1000 genomes] |
rs10022114 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10025149 | 1.00[ASN][1000 genomes] |
rs10025408 | 0.82[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10029349 | 1.00[ASN][1000 genomes] |
rs10034637 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11933728 | 1.00[ASN][1000 genomes] |
rs11937272 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11938668 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11938992 | 1.00[ASN][1000 genomes] |
rs11940945 | 1.00[ASN][1000 genomes] |
rs11941449 | 1.00[ASN][1000 genomes] |
rs13328057 | 1.00[ASN][1000 genomes] |
rs1485012 | 1.00[ASN][1000 genomes] |
rs1485019 | 1.00[ASN][1000 genomes] |
rs1485022 | 0.81[EUR][1000 genomes] |
rs1485024 | 0.81[EUR][1000 genomes] |
rs17020544 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17020556 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17020564 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17020586 | 1.00[ASN][1000 genomes] |
rs17020587 | 1.00[ASN][1000 genomes] |
rs17020631 | 0.85[ASN][1000 genomes] |
rs17020639 | 0.85[ASN][1000 genomes] |
rs17272388 | 0.81[EUR][1000 genomes] |
rs17330789 | 0.81[EUR][1000 genomes] |
rs1905707 | 0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1905708 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1905709 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1905734 | 1.00[ASN][1000 genomes] |
rs1948017 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1948018 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1994252 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1994253 | 1.00[ASN][1000 genomes] |
rs2082553 | 0.81[EUR][1000 genomes] |
rs28480348 | 0.83[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28683046 | 0.83[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28768784 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57028846 | 1.00[ASN][1000 genomes] |
rs60524906 | 1.00[ASN][1000 genomes] |
rs61661603 | 1.00[ASN][1000 genomes] |
rs6532407 | 0.85[ASN][1000 genomes] |
rs6820985 | 1.00[ASN][1000 genomes] |
rs6848749 | 0.85[ASN][1000 genomes] |
rs72884535 | 1.00[ASN][1000 genomes] |
rs72884566 | 0.81[EUR][1000 genomes] |
rs72884570 | 1.00[ASN][1000 genomes] |
rs72884576 | 1.00[ASN][1000 genomes] |
rs72884579 | 1.00[ASN][1000 genomes] |
rs72884580 | 1.00[ASN][1000 genomes] |
rs72884583 | 1.00[ASN][1000 genomes] |
rs72884591 | 1.00[ASN][1000 genomes] |
rs72886215 | 1.00[ASN][1000 genomes] |
rs72886224 | 0.85[ASN][1000 genomes] |
rs7655758 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7662289 | 1.00[ASN][1000 genomes] |
rs7667044 | 1.00[ASN][1000 genomes] |
rs7670552 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7676623 | 1.00[ASN][1000 genomes] |
rs7688091 | 0.84[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7691929 | 1.00[ASN][1000 genomes] |
rs7694361 | 1.00[ASN][1000 genomes] |
rs7695982 | 1.00[ASN][1000 genomes] |
rs9307123 | 1.00[ASN][1000 genomes] |
rs9631716 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs9790383 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9992229 | 0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9998583 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1013255 | chr4:94027129-94462345 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv2830401 | chr4:94141655-94450106 | Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv3584808 | chr4:94156602-94559327 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1008055 | chr4:94169131-95030074 | Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv533846 | chr4:94264488-94462921 | Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv931979 | chr4:94289958-95121723 | Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:94330400-94337800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
2 | chr4:94336600-94338200 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
3 | chr4:94337000-94338000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
4 | chr4:94337200-94337600 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
5 | chr4:94337200-94338600 | Enhancers | Brain Germinal Matrix | brain |
6 | chr4:94337400-94337800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
7 | chr4:94337400-94338000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
8 | chr4:94337400-94338200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
9 | chr4:94337400-94338600 | Enhancers | Cortex derived primary cultured neurospheres | brain |