Variant report
Variant | rs4734729 |
---|---|
Chromosome Location | chr8:104771175-104771176 |
allele | C/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 | chr8:104768356..104771243-chr8:104784970..104787435,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10086733 | 0.96[YRI][hapmap] |
rs10086828 | 0.88[AFR][1000 genomes] |
rs10090039 | 0.90[AFR][1000 genomes] |
rs10090341 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs10091089 | 0.90[AFR][1000 genomes] |
rs10091859 | 0.88[AFR][1000 genomes] |
rs10092889 | 0.96[AFR][1000 genomes] |
rs10096287 | 0.94[AFR][1000 genomes] |
rs10096428 | 0.86[AFR][1000 genomes] |
rs10097302 | 0.98[EUR][1000 genomes] |
rs10100599 | 0.90[AFR][1000 genomes] |
rs10101232 | 0.93[AFR][1000 genomes] |
rs10101275 | 0.90[AFR][1000 genomes] |
rs10102149 | 0.94[AFR][1000 genomes] |
rs10102523 | 0.96[YRI][hapmap] |
rs10103024 | 0.88[AFR][1000 genomes] |
rs10103086 | 0.88[AFR][1000 genomes] |
rs10105191 | 0.88[AFR][1000 genomes] |
rs10105760 | 0.93[AFR][1000 genomes] |
rs10106702 | 0.80[AFR][1000 genomes] |
rs10108212 | 0.90[AFR][1000 genomes] |
rs10110162 | 0.90[AFR][1000 genomes] |
rs10110452 | 0.92[AFR][1000 genomes] |
rs10112260 | 0.92[AFR][1000 genomes] |
rs10113157 | 0.90[AFR][1000 genomes] |
rs10283176 | 0.90[AFR][1000 genomes] |
rs10453069 | 0.84[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs10505046 | 0.95[YRI][hapmap] |
rs10505051 | 0.84[AFR][1000 genomes] |
rs11775418 | 0.94[AFR][1000 genomes] |
rs11776671 | 0.92[AFR][1000 genomes] |
rs11776707 | 0.88[AFR][1000 genomes] |
rs11778502 | 0.90[AFR][1000 genomes] |
rs11779043 | 0.92[AFR][1000 genomes] |
rs11784812 | 0.86[AFR][1000 genomes] |
rs11787180 | 0.88[AFR][1000 genomes] |
rs12156411 | 0.97[EUR][1000 genomes] |
rs12334431 | 0.88[AFR][1000 genomes] |
rs12334852 | 0.92[AFR][1000 genomes] |
rs12334941 | 0.88[AFR][1000 genomes] |
rs12335100 | 0.91[AFR][1000 genomes] |
rs12335106 | 0.88[AFR][1000 genomes] |
rs12335323 | 0.90[AFR][1000 genomes] |
rs12386839 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12681238 | 0.94[EUR][1000 genomes] |
rs12681517 | 0.87[EUR][1000 genomes] |
rs12681640 | 0.97[EUR][1000 genomes] |
rs12707788 | 0.88[AFR][1000 genomes] |
rs12707789 | 0.90[AFR][1000 genomes] |
rs12707790 | 0.90[AFR][1000 genomes] |
rs12707793 | 0.92[AFR][1000 genomes] |
rs12707794 | 0.92[AFR][1000 genomes] |
rs13249502 | 0.88[AFR][1000 genomes] |
rs13249634 | 1.00[YRI][hapmap];0.96[AFR][1000 genomes] |
rs13257824 | 0.90[AFR][1000 genomes] |
rs13259857 | 0.90[AFR][1000 genomes] |
rs13260896 | 0.86[AFR][1000 genomes] |
rs13262003 | 0.90[AFR][1000 genomes] |
rs13262669 | 0.90[AFR][1000 genomes] |
rs13262743 | 0.81[AFR][1000 genomes] |
rs13263306 | 0.88[AFR][1000 genomes] |
rs13273331 | 0.96[AFR][1000 genomes] |
rs13273514 | 0.96[AFR][1000 genomes] |
rs13276150 | 0.88[AFR][1000 genomes] |
rs13279952 | 0.85[AFR][1000 genomes] |
rs13280576 | 0.84[AFR][1000 genomes] |
rs13439565 | 0.93[AFR][1000 genomes] |
rs13439652 | 0.88[AFR][1000 genomes] |
rs13439734 | 0.88[AFR][1000 genomes] |
rs1426288 | 0.85[EUR][1000 genomes] |
rs1426296 | 0.90[AFR][1000 genomes] |
rs1521058 | 0.90[AFR][1000 genomes] |
rs1521064 | 0.94[EUR][1000 genomes] |
rs1593491 | 0.90[AFR][1000 genomes] |
rs1593492 | 0.90[AFR][1000 genomes] |
rs1593493 | 0.90[AFR][1000 genomes] |
rs1593500 | 0.90[AFR][1000 genomes] |
rs16870614 | 1.00[YRI][hapmap];0.88[AFR][1000 genomes] |
rs16870616 | 1.00[YRI][hapmap];0.88[AFR][1000 genomes] |
rs16870641 | 0.92[AFR][1000 genomes] |
rs16870665 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16870826 | 0.86[CEU][hapmap] |
rs17233499 | 0.94[EUR][1000 genomes] |
rs17234011 | 0.97[EUR][1000 genomes] |
rs17234389 | 1.00[YRI][hapmap];0.88[AFR][1000 genomes] |
rs17234965 | 0.97[EUR][1000 genomes] |
rs17234986 | 0.97[EUR][1000 genomes] |
rs17235384 | 0.96[AFR][1000 genomes] |
rs17235420 | 0.96[AFR][1000 genomes] |
rs17806929 | 0.85[EUR][1000 genomes] |
rs17807832 | 0.97[EUR][1000 genomes] |
rs17807953 | 0.97[EUR][1000 genomes] |
rs17808942 | 0.94[AFR][1000 genomes] |
rs1895896 | 0.98[EUR][1000 genomes] |
rs1895898 | 0.97[EUR][1000 genomes] |
rs2080608 | 0.90[AFR][1000 genomes] |
rs2111491 | 0.88[AFR][1000 genomes] |
rs2114249 | 0.97[EUR][1000 genomes] |
rs2160713 | 0.88[AFR][1000 genomes] |
rs2388725 | 0.97[EUR][1000 genomes] |
rs2388781 | 0.90[AFR][1000 genomes] |
rs28420723 | 0.88[AFR][1000 genomes] |
rs28422794 | 0.84[AFR][1000 genomes] |
rs28478652 | 0.94[AFR][1000 genomes] |
rs28515901 | 0.96[AFR][1000 genomes] |
rs28517319 | 0.90[AFR][1000 genomes] |
rs28522982 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs28638005 | 0.96[AFR][1000 genomes] |
rs28667874 | 0.91[EUR][1000 genomes] |
rs28674864 | 0.85[AFR][1000 genomes] |
rs28693917 | 0.87[AFR][1000 genomes] |
rs28772965 | 0.88[AFR][1000 genomes] |
rs28796041 | 0.94[AFR][1000 genomes] |
rs28799635 | 0.86[AFR][1000 genomes] |
rs28846684 | 0.90[AFR][1000 genomes] |
rs28857239 | 0.90[AFR][1000 genomes] |
rs34353892 | 0.88[AFR][1000 genomes] |
rs34955447 | 0.88[AFR][1000 genomes] |
rs34995326 | 0.88[AFR][1000 genomes] |
rs35287474 | 0.92[AFR][1000 genomes] |
rs35294891 | 0.88[AFR][1000 genomes] |
rs35381068 | 0.90[AFR][1000 genomes] |
rs35585808 | 0.90[AFR][1000 genomes] |
rs35732252 | 0.88[AFR][1000 genomes] |
rs35880303 | 0.92[AFR][1000 genomes] |
rs4472479 | 0.97[EUR][1000 genomes] |
rs4734076 | 0.85[EUR][1000 genomes] |
rs4734080 | 1.00[EUR][1000 genomes] |
rs4734728 | 0.94[AFR][1000 genomes] |
rs4734730 | 0.94[AFR][1000 genomes] |
rs4734731 | 0.90[AFR][1000 genomes] |
rs4734734 | 0.91[EUR][1000 genomes] |
rs55731986 | 0.90[AFR][1000 genomes] |
rs55915215 | 0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs56345763 | 0.88[AFR][1000 genomes] |
rs56378194 | 0.92[AFR][1000 genomes] |
rs56999386 | 0.88[AFR][1000 genomes] |
rs58594820 | 0.88[AFR][1000 genomes] |
rs60412815 | 0.81[AFR][1000 genomes] |
rs61589769 | 0.81[AFR][1000 genomes] |
rs6468885 | 0.92[AFR][1000 genomes] |
rs6468886 | 0.92[AFR][1000 genomes] |
rs6468889 | 0.94[AFR][1000 genomes] |
rs6468890 | 0.96[AFR][1000 genomes] |
rs66604513 | 0.90[AFR][1000 genomes] |
rs66631289 | 0.92[AFR][1000 genomes] |
rs66906001 | 0.92[AFR][1000 genomes] |
rs66956359 | 0.90[AFR][1000 genomes] |
rs67220620 | 0.92[AFR][1000 genomes] |
rs67607591 | 0.92[AFR][1000 genomes] |
rs67785072 | 0.82[AFR][1000 genomes] |
rs6982513 | 0.92[AFR][1000 genomes] |
rs6982815 | 0.92[AFR][1000 genomes] |
rs6985107 | 0.94[AFR][1000 genomes] |
rs6985351 | 1.00[YRI][hapmap];0.88[AFR][1000 genomes] |
rs6985447 | 0.90[AFR][1000 genomes] |
rs6986283 | 1.00[YRI][hapmap];0.87[AFR][1000 genomes] |
rs6986976 | 0.90[AFR][1000 genomes] |
rs6987298 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6989899 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6991695 | 0.90[AFR][1000 genomes] |
rs6992080 | 0.94[AFR][1000 genomes] |
rs6992377 | 0.88[AFR][1000 genomes] |
rs6993208 | 0.90[AFR][1000 genomes] |
rs6993536 | 0.87[AFR][1000 genomes] |
rs6993909 | 0.90[AFR][1000 genomes] |
rs7002230 | 0.92[AFR][1000 genomes] |
rs7003269 | 0.94[AFR][1000 genomes] |
rs7004346 | 0.83[YRI][hapmap] |
rs7005828 | 0.88[AFR][1000 genomes] |
rs7012874 | 0.88[AFR][1000 genomes] |
rs7014784 | 0.90[AFR][1000 genomes] |
rs7014799 | 0.90[AFR][1000 genomes] |
rs7014867 | 0.90[AFR][1000 genomes] |
rs7015973 | 0.88[AFR][1000 genomes] |
rs7016776 | 0.94[AFR][1000 genomes] |
rs7016802 | 0.90[AFR][1000 genomes] |
rs7016905 | 0.88[AFR][1000 genomes] |
rs7017726 | 0.94[AFR][1000 genomes] |
rs7018187 | 0.84[AFR][1000 genomes] |
rs71512488 | 0.86[AFR][1000 genomes] |
rs73696700 | 0.92[AFR][1000 genomes] |
rs73697612 | 0.92[AFR][1000 genomes] |
rs73697653 | 0.81[AFR][1000 genomes] |
rs73697657 | 0.83[AFR][1000 genomes] |
rs73697662 | 0.81[AFR][1000 genomes] |
rs73697668 | 0.81[AFR][1000 genomes] |
rs73697700 | 0.81[AFR][1000 genomes] |
rs73701884 | 0.84[AFR][1000 genomes] |
rs769134 | 0.97[EUR][1000 genomes] |
rs7813212 | 0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7818497 | 0.88[AFR][1000 genomes] |
rs7818836 | 0.91[AFR][1000 genomes] |
rs7822017 | 0.90[AFR][1000 genomes] |
rs7824485 | 0.91[AFR][1000 genomes] |
rs7825033 | 0.82[AFR][1000 genomes] |
rs7825696 | 0.90[AFR][1000 genomes] |
rs7832329 | 0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7832358 | 0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7834353 | 0.90[AFR][1000 genomes] |
rs7835266 | 0.88[AFR][1000 genomes] |
rs7835783 | 0.92[AFR][1000 genomes] |
rs7838295 | 0.90[AFR][1000 genomes] |
rs7840564 | 0.88[AFR][1000 genomes] |
rs7842231 | 0.96[AFR][1000 genomes] |
rs7843709 | 0.90[AFR][1000 genomes] |
rs7843860 | 0.89[AFR][1000 genomes] |
rs7843928 | 0.90[AFR][1000 genomes] |
rs7844638 | 0.94[AFR][1000 genomes] |
rs7844822 | 0.94[AFR][1000 genomes] |
rs7845290 | 0.96[YRI][hapmap] |
rs7845768 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9297334 | 0.96[YRI][hapmap] |
rs9297335 | 0.96[YRI][hapmap] |
rs9297336 | 0.88[AFR][1000 genomes] |
rs9297338 | 0.88[AFR][1000 genomes] |
rs9650008 | 0.96[AFR][1000 genomes] |
rs9656788 | 0.92[AFR][1000 genomes] |
rs9918740 | 0.81[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv429931 | chr8:104097396-104878014 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 82 gene(s) | inside rSNPs | diseases |
2 | nsv1020476 | chr8:104312212-104924482 | Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
3 | nsv539704 | chr8:104312212-104924482 | Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
4 | nsv1023048 | chr8:104355188-104872701 | Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
5 | nsv539705 | chr8:104355188-104872701 | ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
6 | nsv1021345 | chr8:104361854-104879684 | Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
7 | nsv1032085 | chr8:104362187-104878345 | Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
8 | nsv1034183 | chr8:104369940-104814008 | Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
9 | nsv539707 | chr8:104369940-104814008 | Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
10 | esv2752692 | chr8:104520824-105123824 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
11 | nsv1016387 | chr8:104578389-104931853 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
12 | nsv1031195 | chr8:104601231-105194208 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive region | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:104750400-104778600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr8:104757000-104780400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr8:104767800-104772800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
4 | chr8:104770200-104772600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
5 | chr8:104770200-104784000 | Weak transcription | H1 Cell Line | embryonic stem cell |
6 | chr8:104770600-104778600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |