Variant report
Variant | rs6833006 |
---|---|
Chromosome Location | chr4:80007345-80007346 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:6)
- 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 | chr4:79998907..80000572-chr4:80006530..80008071,2 | K562 | blood: |
(count:6 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-BMP2K-1 | chr4:80007250-80007416 | ENSG00000249307.1 |
2 | lnc-BMP2K-1 | chr4:80007250-80007416 | ENSG00000249307.1 |
3 | lnc-BMP2K-1 | chr4:80007250-80007416 | ENSG00000249307.1 |
4 | lnc-BMP2K-1 | chr4:80007250-80007416 | NONHSAT097098 |
5 | lnc-BMP2K-1 | chr4:80007244-80007416 | NONHSAT097101 |
6 | lnc-BMP2K-1 | chr4:80007244-80007416 | NONHSAT097102 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10518213 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11723369 | 0.99[EUR][1000 genomes] |
rs12499521 | 0.98[EUR][1000 genomes] |
rs12643284 | 0.96[EUR][1000 genomes] |
rs1350008 | 1.00[EUR][1000 genomes] |
rs1378379 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1455299 | 1.00[EUR][1000 genomes] |
rs1455305 | 0.98[EUR][1000 genomes] |
rs1455306 | 0.98[EUR][1000 genomes] |
rs1455307 | 0.98[EUR][1000 genomes] |
rs1480719 | 0.95[EUR][1000 genomes] |
rs1480735 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1480736 | 0.97[EUR][1000 genomes] |
rs1480737 | 0.97[EUR][1000 genomes] |
rs1480738 | 1.00[EUR][1000 genomes] |
rs17003589 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs17003625 | 1.00[CEU][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17003626 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs188253 | 0.99[EUR][1000 genomes] |
rs188254 | 0.99[EUR][1000 genomes] |
rs2016189 | 1.00[EUR][1000 genomes] |
rs207020 | 0.99[EUR][1000 genomes] |
rs2127782 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2127783 | 1.00[EUR][1000 genomes] |
rs2604827 | 1.00[EUR][1000 genomes] |
rs2604828 | 0.98[EUR][1000 genomes] |
rs2604829 | 0.82[EUR][1000 genomes] |
rs2604830 | 0.98[EUR][1000 genomes] |
rs2604832 | 0.96[EUR][1000 genomes] |
rs2604833 | 0.97[EUR][1000 genomes] |
rs2604834 | 0.98[EUR][1000 genomes] |
rs2622350 | 0.98[EUR][1000 genomes] |
rs2622352 | 0.97[EUR][1000 genomes] |
rs2622353 | 0.96[EUR][1000 genomes] |
rs2622354 | 0.97[EUR][1000 genomes] |
rs2622355 | 0.91[EUR][1000 genomes] |
rs2622356 | 0.93[EUR][1000 genomes] |
rs2622357 | 0.98[EUR][1000 genomes] |
rs2622358 | 1.00[EUR][1000 genomes] |
rs286448 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs286450 | 0.80[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs286452 | 0.95[EUR][1000 genomes] |
rs286456 | 0.97[EUR][1000 genomes] |
rs286457 | 0.97[EUR][1000 genomes] |
rs286458 | 0.96[EUR][1000 genomes] |
rs286459 | 0.91[EUR][1000 genomes] |
rs286460 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs286461 | 0.99[EUR][1000 genomes] |
rs286462 | 0.99[EUR][1000 genomes] |
rs286463 | 0.80[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs286464 | 0.99[EUR][1000 genomes] |
rs286465 | 0.99[EUR][1000 genomes] |
rs286466 | 0.98[EUR][1000 genomes] |
rs286467 | 0.98[EUR][1000 genomes] |
rs286468 | 0.98[EUR][1000 genomes] |
rs286473 | 0.84[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs4320158 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs55672352 | 1.00[EUR][1000 genomes] |
rs56391107 | 1.00[EUR][1000 genomes] |
rs62308747 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62308748 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62308749 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62310026 | 0.83[EUR][1000 genomes] |
rs6813045 | 1.00[EUR][1000 genomes] |
rs6813727 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6825891 | 1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6838863 | 1.00[EUR][1000 genomes] |
rs7438158 | 1.00[CEU][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7685661 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs930834 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs962169 | 1.00[EUR][1000 genomes] |
rs9686053 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv829979 | chr4:79819168-80019159 | Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
2 | nsv1000907 | chr4:79838948-80224764 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
3 | nsv879505 | chr4:79887043-80293046 | Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | esv3448470 | chr4:79898340-80026510 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:80005000-80007600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
2 | chr4:80005400-80009400 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
3 | chr4:80005800-80010000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr4:80006400-80010000 | Weak transcription | Fetal Heart | heart |
5 | chr4:80007200-80007400 | Enhancers | Colon Smooth Muscle | Colon |
6 | chr4:80007200-80011200 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
7 | chr4:80007200-80012400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |