Variant report
Variant | rs17169237 |
---|---|
Chromosome Location | chr7:137228885-137228886 |
allele | A/C |
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 | chr7:137226774..137229451-chr7:137231798..137234078,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10081252 | 1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs10226970 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10229086 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10232182 | 0.89[EUR][1000 genomes] |
rs10233537 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10234462 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10237704 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10238276 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10238305 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10242081 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10242488 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10242747 | 0.89[EUR][1000 genomes] |
rs10245413 | 0.89[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs10246490 | 0.89[EUR][1000 genomes] |
rs10246829 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10246952 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10252668 | 0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10255388 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10255937 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10260210 | 1.00[EUR][1000 genomes] |
rs10260958 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10261618 | 0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];1.00[EUR][1000 genomes] |
rs10264172 | 1.00[JPT][hapmap];1.00[EUR][1000 genomes] |
rs10264413 | 0.94[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs10268521 | 0.89[EUR][1000 genomes] |
rs10271043 | 0.89[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10273321 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10274366 | 0.89[EUR][1000 genomes] |
rs10274702 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10277872 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10279489 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs10280229 | 1.00[JPT][hapmap] |
rs10281244 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs1358445 | 1.00[EUR][1000 genomes] |
rs1358446 | 1.00[EUR][1000 genomes] |
rs1358447 | 1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs1364367 | 0.89[EUR][1000 genomes] |
rs1525043 | 0.89[EUR][1000 genomes] |
rs1525044 | 0.89[EUR][1000 genomes] |
rs1525046 | 0.89[EUR][1000 genomes] |
rs1525047 | 0.89[EUR][1000 genomes] |
rs1525049 | 0.95[GIH][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs1614024 | 0.89[EUR][1000 genomes] |
rs1615692 | 0.89[EUR][1000 genomes] |
rs1629172 | 0.89[EUR][1000 genomes] |
rs1646364 | 0.89[EUR][1000 genomes] |
rs1646371 | 0.89[EUR][1000 genomes] |
rs1646372 | 1.00[GIH][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs1646373 | 0.89[EUR][1000 genomes] |
rs1646375 | 1.00[GIH][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs1646376 | 0.89[EUR][1000 genomes] |
rs1646377 | 0.89[EUR][1000 genomes] |
rs1646378 | 0.89[EUR][1000 genomes] |
rs1646380 | 0.89[EUR][1000 genomes] |
rs1646381 | 0.89[EUR][1000 genomes] |
rs1646382 | 0.89[EUR][1000 genomes] |
rs1646383 | 0.89[EUR][1000 genomes] |
rs1646384 | 0.89[EUR][1000 genomes] |
rs1646385 | 0.89[EUR][1000 genomes] |
rs1646386 | 0.89[EUR][1000 genomes] |
rs1646387 | 0.89[EUR][1000 genomes] |
rs1646388 | 0.89[EUR][1000 genomes] |
rs1646389 | 0.94[GIH][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs1646390 | 0.89[EUR][1000 genomes] |
rs1646393 | 0.89[EUR][1000 genomes] |
rs1646395 | 0.89[EUR][1000 genomes] |
rs1646397 | 0.89[EUR][1000 genomes] |
rs1646400 | 0.89[EUR][1000 genomes] |
rs1646401 | 0.89[EUR][1000 genomes] |
rs17169262 | 0.89[EUR][1000 genomes] |
rs17169284 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs17169298 | 0.85[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs17169313 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs17169324 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs1723086 | 0.89[EUR][1000 genomes] |
rs1723088 | 0.89[EUR][1000 genomes] |
rs1723089 | 0.89[EUR][1000 genomes] |
rs1723090 | 0.89[EUR][1000 genomes] |
rs1723091 | 0.89[EUR][1000 genomes] |
rs1723094 | 0.89[EUR][1000 genomes] |
rs1723095 | 0.89[EUR][1000 genomes] |
rs1723096 | 0.89[EUR][1000 genomes] |
rs1723101 | 0.89[EUR][1000 genomes] |
rs1723102 | 0.89[EUR][1000 genomes] |
rs1723103 | 0.89[EUR][1000 genomes] |
rs1723104 | 0.89[EUR][1000 genomes] |
rs1723106 | 0.89[EUR][1000 genomes] |
rs1723107 | 0.89[EUR][1000 genomes] |
rs1723109 | 0.89[EUR][1000 genomes] |
rs1723119 | 0.89[EUR][1000 genomes] |
rs1723120 | 0.89[EUR][1000 genomes] |
rs1723122 | 0.89[EUR][1000 genomes] |
rs1723123 | 0.89[EUR][1000 genomes] |
rs1728441 | 0.89[EUR][1000 genomes] |
rs1728442 | 0.89[EUR][1000 genomes] |
rs1728443 | 1.00[GIH][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs1728450 | 1.00[JPT][hapmap] |
rs1728453 | 1.00[JPT][hapmap] |
rs1728476 | 1.00[EUR][1000 genomes] |
rs1728491 | 0.89[EUR][1000 genomes] |
rs1728493 | 0.89[EUR][1000 genomes] |
rs1728495 | 0.89[EUR][1000 genomes] |
rs1728496 | 0.89[EUR][1000 genomes] |
rs1728497 | 0.89[EUR][1000 genomes] |
rs1728498 | 0.94[GIH][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs2293547 | 1.00[EUR][1000 genomes] |
rs2293548 | 1.00[EUR][1000 genomes] |
rs2550979 | 0.89[EUR][1000 genomes] |
rs2550981 | 0.89[EUR][1000 genomes] |
rs2692001 | 0.89[EUR][1000 genomes] |
rs2692002 | 0.89[EUR][1000 genomes] |
rs2692003 | 0.89[EUR][1000 genomes] |
rs2692006 | 0.89[EUR][1000 genomes] |
rs2692007 | 0.89[EUR][1000 genomes] |
rs2692008 | 0.94[GIH][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes] |
rs28401380 | 1.00[EUR][1000 genomes] |
rs28451058 | 0.89[EUR][1000 genomes] |
rs28521198 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28572056 | 0.89[EUR][1000 genomes] |
rs28711988 | 1.00[EUR][1000 genomes] |
rs28736349 | 0.89[EUR][1000 genomes] |
rs28755996 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs28758372 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3800605 | 0.83[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs3800609 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs3800610 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs3800611 | 1.00[JPT][hapmap] |
rs3823545 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs3823547 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs57226761 | 0.89[EUR][1000 genomes] |
rs58048755 | 0.89[EUR][1000 genomes] |
rs59024585 | 1.00[EUR][1000 genomes] |
rs6945142 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6945473 | 1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6946246 | 1.00[EUR][1000 genomes] |
rs6949210 | 0.89[EUR][1000 genomes] |
rs6949568 | 0.89[EUR][1000 genomes] |
rs6963894 | 1.00[EUR][1000 genomes] |
rs6964439 | 1.00[EUR][1000 genomes] |
rs6964837 | 1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs6969227 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs6969358 | 0.89[EUR][1000 genomes] |
rs697596 | 1.00[JPT][hapmap] |
rs706560 | 1.00[JPT][hapmap] |
rs706561 | 0.89[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs706562 | 1.00[JPT][hapmap] |
rs706567 | 1.00[JPT][hapmap] |
rs706568 | 1.00[JPT][hapmap] |
rs73449424 | 1.00[EUR][1000 genomes] |
rs73449434 | 1.00[EUR][1000 genomes] |
rs73449444 | 0.89[EUR][1000 genomes] |
rs73451467 | 0.89[EUR][1000 genomes] |
rs73453511 | 0.89[EUR][1000 genomes] |
rs73453514 | 0.89[EUR][1000 genomes] |
rs73453584 | 0.89[EUR][1000 genomes] |
rs73453598 | 0.89[EUR][1000 genomes] |
rs73728732 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7781327 | 0.85[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.89[EUR][1000 genomes] |
rs7800321 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs834051 | 0.89[EUR][1000 genomes] |
rs834052 | 0.89[EUR][1000 genomes] |
rs834054 | 1.00[GIH][hapmap];0.89[EUR][1000 genomes] |
rs834055 | 0.89[EUR][1000 genomes] |
rs834056 | 0.89[EUR][1000 genomes] |
rs834057 | 0.89[EUR][1000 genomes] |
rs834058 | 0.89[EUR][1000 genomes] |
rs834069 | 1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs834077 | 0.89[EUR][1000 genomes] |
rs834078 | 0.89[EUR][1000 genomes] |
rs834086 | 1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs834095 | 0.89[EUR][1000 genomes] |
rs834099 | 1.00[JPT][hapmap] |
rs834100 | 1.00[JPT][hapmap] |
rs834439 | 0.85[CHD][hapmap];1.00[JPT][hapmap] |
rs834444 | 1.00[JPT][hapmap] |
rs834447 | 1.00[JPT][hapmap] |
rs863082 | 1.00[JPT][hapmap] |
rs865021 | 0.89[EUR][1000 genomes] |
rs883222 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869820 | chr7:136990386-137347718 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1027868 | chr7:137004690-137311653 | Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
3 | nsv539134 | chr7:137004690-137311653 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
4 | nsv1022793 | chr7:137187383-137619359 | Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:137207200-137232600 | Weak transcription | Aorta | Aorta |
2 | chr7:137215400-137275400 | Weak transcription | Brain Angular Gyrus | brain |
3 | chr7:137216600-137236600 | Weak transcription | Brain Anterior Caudate | brain |
4 | chr7:137224200-137236200 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
5 | chr7:137224400-137274800 | Weak transcription | HSMMtube | muscle |
6 | chr7:137224600-137232400 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
7 | chr7:137224800-137262400 | Weak transcription | HSMM | muscle |
8 | chr7:137225000-137229600 | Weak transcription | Muscle Satellite Cultured Cells | -- |
9 | chr7:137225000-137231400 | Weak transcription | Osteobl | bone |
10 | chr7:137225000-137232600 | Weak transcription | NH-A | brain |
11 | chr7:137225200-137231400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
12 | chr7:137225600-137232400 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
13 | chr7:137225800-137240600 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
14 | chr7:137228600-137230800 | Strong transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
15 | chr7:137228800-137231600 | Enhancers | Fetal Stomach | stomach |