Variant report
Variant | rs11633974 |
---|---|
Chromosome Location | chr15:39927152-39927153 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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rs_ID | r2[population] |
---|---|
rs1004739 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1004740 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1004741 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10520135 | 0.87[CEU][hapmap] |
rs10520137 | 1.00[CEU][hapmap] |
rs11070220 | 1.00[CEU][hapmap] |
rs11070222 | 1.00[CEU][hapmap] |
rs11070223 | 1.00[CEU][hapmap] |
rs11070225 | 1.00[CEU][hapmap] |
rs1134485 | 1.00[CEU][hapmap] |
rs11630406 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs11631570 | 1.00[CEU][hapmap];0.94[CHB][hapmap] |
rs11632879 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs11635103 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs11638041 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs11638500 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs11638558 | 0.98[AFR][1000 genomes] |
rs11852591 | 1.00[CEU][hapmap];0.81[JPT][hapmap] |
rs11852649 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs11854797 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap] |
rs11856294 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11856448 | 0.88[CHB][hapmap] |
rs11856971 | 1.00[CEU][hapmap] |
rs11857819 | 1.00[CEU][hapmap] |
rs11857927 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12908846 | 1.00[CEU][hapmap] |
rs12912082 | 1.00[CEU][hapmap] |
rs16969386 | 1.00[CEU][hapmap] |
rs16969410 | 1.00[CEU][hapmap] |
rs16969445 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs16969459 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs16969460 | 1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs16969475 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[MKK][hapmap];0.82[TSI][hapmap] |
rs16969478 | 1.00[CEU][hapmap];0.86[GIH][hapmap];0.86[MKK][hapmap];0.86[TSI][hapmap] |
rs16969495 | 0.89[CHB][hapmap] |
rs16969637 | 0.89[CHB][hapmap] |
rs16969640 | 0.89[CHB][hapmap] |
rs1876853 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[MKK][hapmap];0.86[TSI][hapmap] |
rs2228261 | 1.00[CEU][hapmap] |
rs2292305 | 1.00[CEU][hapmap] |
rs2411312 | 0.90[TSI][hapmap];0.81[EUR][1000 genomes] |
rs2411313 | 1.00[CEU][hapmap] |
rs2412409 | 1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2412410 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2412411 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2412413 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[TSI][hapmap] |
rs2412415 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs2412417 | 1.00[CEU][hapmap];0.81[JPT][hapmap] |
rs2412419 | 1.00[CEU][hapmap] |
rs2898686 | 1.00[CEU][hapmap] |
rs2898687 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[MKK][hapmap];0.86[TSI][hapmap] |
rs2898688 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs34275067 | 0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs35754803 | 0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3784390 | 1.00[CEU][hapmap];0.82[GIH][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes] |
rs4349120 | 1.00[CEU][hapmap];0.82[JPT][hapmap] |
rs4476147 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4547308 | 1.00[CEU][hapmap];0.81[JPT][hapmap] |
rs4583211 | 1.00[CEU][hapmap];0.81[JPT][hapmap] |
rs56722485 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs57969006 | 0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs58332880 | 0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs60884629 | 0.91[EUR][1000 genomes] |
rs7162070 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[MKK][hapmap];0.86[TSI][hapmap] |
rs7162781 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[TSI][hapmap] |
rs7167184 | 1.00[CEU][hapmap] |
rs7168755 | 1.00[CEU][hapmap];0.81[JPT][hapmap] |
rs7169478 | 1.00[CEU][hapmap] |
rs7169574 | 1.00[CEU][hapmap] |
rs72725045 | 0.87[EUR][1000 genomes] |
rs753599 | 1.00[CEU][hapmap] |
rs8029602 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[MKK][hapmap];0.86[TSI][hapmap] |
rs8032035 | 1.00[CEU][hapmap] |
rs8036376 | 0.88[CEU][hapmap] |
rs8036633 | 0.88[CEU][hapmap] |
rs884584 | 1.00[CEU][hapmap];0.87[GIH][hapmap];0.86[TSI][hapmap] |
rs999393 | 0.81[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1049682 | chr15:39657279-40027403 | Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
2 | nsv542361 | chr15:39657279-40027403 | Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
3 | esv3373125 | chr15:39691567-40061262 | Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
4 | nsv904094 | chr15:39738006-39976057 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
5 | nsv832977 | chr15:39817512-39981520 | Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
6 | nsv1048628 | chr15:39877498-39940104 | Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
7 | nsv1502 | chr15:39884314-39928968 | Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
8 | nsv832978 | chr15:39899759-40094881 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:39916400-39937800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr15:39921400-39937600 | Weak transcription | Psoas Muscle | Psoas |
3 | chr15:39923800-39939600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
4 | chr15:39924200-39932200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr15:39925400-39929600 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |
6 | chr15:39926400-39934400 | Weak transcription | Pancreas | Pancrea |