Variant report
Variant | rs876464 |
---|---|
Chromosome Location | chr4:110309570-110309571 |
allele | A/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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:110308992..110311628-chr4:110320661..110323611,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10000545 | 0.85[JPT][hapmap] |
rs10002595 | 0.85[JPT][hapmap] |
rs10005198 | 0.94[EUR][1000 genomes] |
rs10007410 | 0.87[EUR][1000 genomes] |
rs10028250 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs10155127 | 0.85[JPT][hapmap] |
rs10155246 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs11098033 | 0.85[JPT][hapmap] |
rs11098035 | 0.85[JPT][hapmap] |
rs11929713 | 0.82[JPT][hapmap] |
rs11930655 | 0.82[JPT][hapmap] |
rs11933172 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs11939924 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11942140 | 0.87[AMR][1000 genomes] |
rs11942291 | 0.85[JPT][hapmap] |
rs11942858 | 0.85[JPT][hapmap] |
rs11943384 | 0.82[JPT][hapmap] |
rs11943430 | 0.85[JPT][hapmap] |
rs12640049 | 0.87[AMR][1000 genomes] |
rs12641197 | 0.89[EUR][1000 genomes] |
rs12641272 | 0.88[EUR][1000 genomes] |
rs12643055 | 0.85[JPT][hapmap] |
rs12648138 | 0.85[JPT][hapmap] |
rs12650654 | 0.85[JPT][hapmap] |
rs13103034 | 0.85[JPT][hapmap] |
rs13104799 | 0.91[EUR][1000 genomes] |
rs13113384 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs13119700 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs13123618 | 0.85[JPT][hapmap] |
rs13126829 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs13138833 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs13143825 | 0.85[JPT][hapmap] |
rs13145066 | 0.85[JPT][hapmap] |
rs1509314 | 0.85[JPT][hapmap] |
rs1509315 | 0.85[JPT][hapmap] |
rs1557804 | 0.89[EUR][1000 genomes] |
rs17040436 | 0.85[JPT][hapmap] |
rs17040439 | 0.85[JPT][hapmap] |
rs17040461 | 0.85[JPT][hapmap] |
rs17585970 | 0.85[JPT][hapmap] |
rs17619262 | 0.85[JPT][hapmap] |
rs17842269 | 0.89[EUR][1000 genomes] |
rs1859144 | 0.90[EUR][1000 genomes] |
rs1859146 | 0.89[EUR][1000 genomes] |
rs1859147 | 0.94[EUR][1000 genomes] |
rs1981540 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs1981541 | 0.89[EUR][1000 genomes] |
rs2079108 | 0.94[EUR][1000 genomes] |
rs2214377 | 0.89[EUR][1000 genomes] |
rs2346014 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs28374470 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs28463999 | 0.89[EUR][1000 genomes] |
rs28542804 | 0.91[EUR][1000 genomes] |
rs28585579 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs28628718 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs28681408 | 0.85[JPT][hapmap] |
rs28749845 | 0.94[EUR][1000 genomes] |
rs4524460 | 0.94[EUR][1000 genomes] |
rs6533426 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6815455 | 0.85[JPT][hapmap] |
rs6818911 | 0.85[JPT][hapmap] |
rs6825928 | 1.00[CEU][hapmap] |
rs6827985 | 0.94[EUR][1000 genomes] |
rs6835683 | 0.85[JPT][hapmap] |
rs6841133 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6841198 | 0.85[JPT][hapmap] |
rs6841222 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6848452 | 0.82[AMR][1000 genomes] |
rs6856291 | 0.85[JPT][hapmap] |
rs7436583 | 0.85[JPT][hapmap];0.82[AMR][1000 genomes] |
rs7436745 | 0.85[JPT][hapmap] |
rs7440570 | 0.85[JPT][hapmap] |
rs7665024 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7673595 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs7673867 | 0.94[EUR][1000 genomes] |
rs7675344 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes] |
rs7675602 | 0.85[JPT][hapmap] |
rs7680752 | 0.89[EUR][1000 genomes] |
rs7680920 | 0.89[EUR][1000 genomes] |
rs7684744 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7685787 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7687245 | 0.85[JPT][hapmap] |
rs7694523 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7695754 | 1.00[CEU][hapmap] |
rs7699247 | 0.84[EUR][1000 genomes] |
rs9307329 | 0.89[EUR][1000 genomes] |
rs9985632 | 0.85[JPT][hapmap] |
rs9985964 | 0.85[JPT][hapmap] |
rs9993228 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9994676 | 0.85[JPT][hapmap] |
rs9996165 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs9996432 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9996537 | 0.89[EUR][1000 genomes] |
rs9996920 | 0.89[EUR][1000 genomes] |
rs9999270 | 0.89[EUR][1000 genomes] |
rs9999278 | 0.89[EUR][1000 genomes] |
rs9999570 | 0.85[JPT][hapmap] |
rs9999751 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv461613 | chr4:109922064-110593460 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
2 | nsv595129 | chr4:109922064-110593460 | Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
3 | esv1799708 | chr4:110309234-110333106 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:110305600-110310600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr4:110306600-110316400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr4:110307800-110310200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
4 | chr4:110307800-110310200 | Weak transcription | Fetal Heart | heart |
5 | chr4:110308400-110310000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
6 | chr4:110308600-110309600 | Enhancers | H9 Cell Line | embryonic stem cell |
7 | chr4:110308800-110310400 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
8 | chr4:110308800-110310600 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
9 | chr4:110309000-110310000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
10 | chr4:110309000-110310000 | Weak transcription | Fetal Muscle Leg | muscle |
11 | chr4:110309200-110310200 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
12 | chr4:110309400-110309600 | Enhancers | Muscle Satellite Cultured Cells | -- |