Variant report
Variant | rs16824458 |
---|---|
Chromosome Location | chr1:185735239-185735240 |
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 | chr1:185735098..185737395-chr1:185742780..185745714,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10047250 | 1.00[CHB][hapmap] |
rs10465500 | 1.00[CHB][hapmap] |
rs10489713 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10489714 | 1.00[CHB][hapmap] |
rs10489715 | 1.00[CHB][hapmap] |
rs10489716 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs10489717 | 1.00[CHB][hapmap] |
rs10911785 | 1.00[CHB][hapmap] |
rs1124755 | 1.00[ASN][1000 genomes] |
rs1124756 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11800990 | 1.00[CHB][hapmap] |
rs12097100 | 1.00[EUR][1000 genomes] |
rs1321671 | 1.00[CHB][hapmap] |
rs1321672 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1321673 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1321674 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1321675 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1407428 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs1555494 | 1.00[CHB][hapmap] |
rs16824426 | 1.00[CHB][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs16824427 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs16824428 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs16824451 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs16824455 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16824465 | 1.00[CHB][hapmap] |
rs16824488 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs16824497 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs16824524 | 1.00[CHB][hapmap] |
rs1825398 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1830622 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs1830623 | 1.00[EUR][1000 genomes] |
rs1853247 | 1.00[EUR][1000 genomes] |
rs2170858 | 1.00[EUR][1000 genomes] |
rs2200266 | 1.00[CHB][hapmap] |
rs28477118 | 1.00[EUR][1000 genomes] |
rs28510615 | 1.00[EUR][1000 genomes] |
rs55731570 | 1.00[EUR][1000 genomes] |
rs55887884 | 1.00[EUR][1000 genomes] |
rs56100961 | 1.00[EUR][1000 genomes] |
rs56331179 | 1.00[EUR][1000 genomes] |
rs56347630 | 1.00[EUR][1000 genomes] |
rs56881574 | 1.00[EUR][1000 genomes] |
rs57036166 | 1.00[EUR][1000 genomes] |
rs57107751 | 1.00[EUR][1000 genomes] |
rs57162167 | 1.00[EUR][1000 genomes] |
rs57215320 | 1.00[EUR][1000 genomes] |
rs57246058 | 1.00[EUR][1000 genomes] |
rs57257586 | 1.00[EUR][1000 genomes] |
rs57646829 | 1.00[EUR][1000 genomes] |
rs57782754 | 1.00[EUR][1000 genomes] |
rs58433773 | 1.00[EUR][1000 genomes] |
rs58610741 | 1.00[EUR][1000 genomes] |
rs59175860 | 1.00[EUR][1000 genomes] |
rs59660733 | 1.00[EUR][1000 genomes] |
rs59967839 | 1.00[EUR][1000 genomes] |
rs60308365 | 1.00[EUR][1000 genomes] |
rs60458315 | 1.00[EUR][1000 genomes] |
rs60735946 | 1.00[EUR][1000 genomes] |
rs61679640 | 1.00[EUR][1000 genomes] |
rs61689983 | 1.00[EUR][1000 genomes] |
rs6425004 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6425005 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6657554 | 1.00[CHB][hapmap] |
rs6657683 | 1.00[CHB][hapmap] |
rs6662653 | 1.00[CHB][hapmap] |
rs6671094 | 1.00[EUR][1000 genomes] |
rs6675691 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6676349 | 1.00[EUR][1000 genomes] |
rs6676522 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6676629 | 1.00[CHB][hapmap];1.00[AMR][1000 genomes] |
rs6676765 | 1.00[CHB][hapmap] |
rs6676937 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6677167 | 1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6677183 | 1.00[EUR][1000 genomes] |
rs6679816 | 1.00[CHB][hapmap];1.00[AMR][1000 genomes] |
rs6683809 | 1.00[CHB][hapmap] |
rs6685093 | 1.00[ASN][1000 genomes] |
rs6688298 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6689228 | 1.00[EUR][1000 genomes] |
rs6689359 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6690475 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6690559 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6690714 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs6696804 | 1.00[CHB][hapmap] |
rs6698721 | 1.00[CHB][hapmap] |
rs6700856 | 1.00[EUR][1000 genomes] |
rs6703750 | 1.00[EUR][1000 genomes] |
rs73054432 | 1.00[EUR][1000 genomes] |
rs73054448 | 1.00[EUR][1000 genomes] |
rs73058398 | 1.00[ASN][1000 genomes] |
rs73058399 | 1.00[ASN][1000 genomes] |
rs73060487 | 1.00[EUR][1000 genomes] |
rs73062512 | 1.00[EUR][1000 genomes] |
rs73062516 | 1.00[EUR][1000 genomes] |
rs73070519 | 1.00[EUR][1000 genomes] |
rs73070522 | 1.00[EUR][1000 genomes] |
rs73070527 | 1.00[EUR][1000 genomes] |
rs73070547 | 1.00[EUR][1000 genomes] |
rs73070548 | 1.00[EUR][1000 genomes] |
rs73070567 | 1.00[EUR][1000 genomes] |
rs73070598 | 1.00[EUR][1000 genomes] |
rs73072012 | 1.00[EUR][1000 genomes] |
rs73072023 | 1.00[EUR][1000 genomes] |
rs73072049 | 1.00[EUR][1000 genomes] |
rs73072063 | 1.00[EUR][1000 genomes] |
rs73072067 | 1.00[EUR][1000 genomes] |
rs74134207 | 1.00[EUR][1000 genomes] |
rs74134210 | 1.00[EUR][1000 genomes] |
rs74134216 | 1.00[EUR][1000 genomes] |
rs74134306 | 1.00[EUR][1000 genomes] |
rs74134381 | 1.00[ASN][1000 genomes] |
rs74135337 | 1.00[EUR][1000 genomes] |
rs74135346 | 1.00[EUR][1000 genomes] |
rs74135350 | 1.00[EUR][1000 genomes] |
rs74135351 | 1.00[EUR][1000 genomes] |
rs74135359 | 1.00[EUR][1000 genomes] |
rs74135362 | 1.00[EUR][1000 genomes] |
rs74135365 | 1.00[EUR][1000 genomes] |
rs7517811 | 1.00[EUR][1000 genomes] |
rs7521401 | 1.00[CHB][hapmap] |
rs7532062 | 1.00[AMR][1000 genomes] |
rs7532816 | 1.00[AMR][1000 genomes] |
rs7540727 | 1.00[CHB][hapmap];1.00[EUR][1000 genomes] |
rs7540773 | 1.00[EUR][1000 genomes] |
rs7541361 | 1.00[CHB][hapmap] |
rs7544162 | 1.00[EUR][1000 genomes] |
rs7544394 | 1.00[EUR][1000 genomes] |
rs7544808 | 1.00[EUR][1000 genomes] |
rs7546152 | 1.00[CHB][hapmap] |
rs7555536 | 1.00[AMR][1000 genomes] |
rs959688 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs959689 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs959690 | 1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv548398 | chr1:185136458-186003094 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 69 gene(s) | inside rSNPs | diseases |
2 | esv3424090 | chr1:185679718-186270877 | Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:185721800-185736400 | Weak transcription | Fetal Lung | lung |
2 | chr1:185730200-185745000 | Weak transcription | Fetal Kidney | kidney |
3 | chr1:185732400-185742800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr1:185733200-185735600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
5 | chr1:185734800-185736000 | Enhancers | Aorta | Aorta |
6 | chr1:185735000-185736600 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |