Variant report
Variant | rs7299984 |
---|---|
Chromosome Location | chr12:73003833-73003834 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs10735970 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10748198 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs10748202 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10784975 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10784978 | 0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10784979 | 0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10879436 | 0.81[EUR][1000 genomes] |
rs10879439 | 0.84[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs10879458 | 0.81[ASN][1000 genomes] |
rs10879459 | 0.82[ASN][1000 genomes] |
rs10879460 | 0.83[ASN][1000 genomes] |
rs10879461 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10879462 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10879464 | 0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10879465 | 0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10879466 | 0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10879472 | 0.90[ASN][1000 genomes] |
rs11179280 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1214894 | 0.93[EUR][1000 genomes] |
rs1214897 | 0.92[EUR][1000 genomes] |
rs1214899 | 0.92[EUR][1000 genomes] |
rs1347194 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1347196 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1353160 | 0.81[EUR][1000 genomes] |
rs1389497 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs1444606 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1444607 | 0.81[EUR][1000 genomes] |
rs1687265 | 0.86[EUR][1000 genomes] |
rs1817885 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs1836042 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1836043 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1836044 | 0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1864837 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1864838 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1965318 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1991751 | 0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs2367747 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2887071 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs305396 | 0.90[ASN][1000 genomes] |
rs305402 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs305403 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs3782366 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs3782367 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs3817612 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs3843025 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3852549 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3852550 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs3910234 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4100196 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs41387445 | 0.83[ASN][1000 genomes] |
rs458942 | 0.87[ASN][1000 genomes] |
rs460406 | 0.90[ASN][1000 genomes] |
rs58509346 | 0.82[ASN][1000 genomes] |
rs58687032 | 0.82[ASN][1000 genomes] |
rs605027 | 0.84[EUR][1000 genomes] |
rs626266 | 0.80[EUR][1000 genomes] |
rs6582090 | 0.81[EUR][1000 genomes] |
rs6582093 | 0.81[ASN][1000 genomes] |
rs6582094 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6582095 | 0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs683101 | 0.85[EUR][1000 genomes] |
rs7131984 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7135547 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs71457035 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs723867 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7308678 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs7309263 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7309651 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7967001 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs7969680 | 0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7969934 | 0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs963407 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs996575 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2422452 | chr12:72485933-73175581 | Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv899257 | chr12:72569746-73145896 | ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
3 | nsv1044083 | chr12:72647640-73275526 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
4 | nsv469465 | chr12:72655925-73259114 | Weak transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
5 | nsv559363 | chr12:72655925-73259114 | Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
6 | nsv868884 | chr12:72664763-73241518 | Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
7 | nsv817280 | chr12:72820558-73508605 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | nsv899259 | chr12:72885554-73011367 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv832454 | chr12:72940798-73081180 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | esv1805187 | chr12:72949787-73013475 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv1054725 | chr12:72990553-73062598 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | esv2758314 | chr12:72990707-73251109 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
13 | esv2759908 | chr12:72990707-73251109 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
14 | nsv868885 | chr12:72998553-73587081 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:73002200-73006000 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
2 | chr12:73002200-73006800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr12:73002400-73004200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
4 | chr12:73002400-73004200 | Weak transcription | Fetal Intestine Large | intestine |
5 | chr12:73002600-73004000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
6 | chr12:73002600-73004000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
7 | chr12:73002600-73004600 | Weak transcription | Ovary | ovary |
8 | chr12:73002800-73004000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
9 | chr12:73003000-73004200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
10 | chr12:73003600-73005600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
11 | chr12:73003600-73007800 | Enhancers | HUES64 Cell Line | embryonic stem cell |
12 | chr12:73003600-73008800 | Enhancers | HUES6 Cell Line | embryonic stem cell |