Variant report
Variant | rs17443178 |
---|---|
Chromosome Location | chr12:40586065-40586066 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:1 , 50 per page) page:
1
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
LRRK2 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10506144 | 0.86[EUR][1000 genomes] |
rs10506147 | 0.80[EUR][1000 genomes] |
rs11174697 | 0.80[EUR][1000 genomes] |
rs11175186 | 0.86[EUR][1000 genomes] |
rs11175593 | 0.80[EUR][1000 genomes] |
rs11564107 | 0.80[EUR][1000 genomes] |
rs11564128 | 1.00[JPT][hapmap] |
rs11564153 | 0.80[EUR][1000 genomes] |
rs11564187 | 0.80[EUR][1000 genomes] |
rs11564199 | 0.80[EUR][1000 genomes] |
rs11564204 | 1.00[JPT][hapmap] |
rs11564210 | 0.80[EUR][1000 genomes] |
rs11564212 | 0.80[EUR][1000 genomes] |
rs11564216 | 0.86[EUR][1000 genomes] |
rs12368785 | 1.00[JPT][hapmap] |
rs12368891 | 1.00[JPT][hapmap] |
rs12422544 | 0.86[EUR][1000 genomes] |
rs12424040 | 0.86[EUR][1000 genomes] |
rs12426378 | 0.86[EUR][1000 genomes] |
rs1388597 | 0.80[EUR][1000 genomes] |
rs17442206 | 1.00[JPT][hapmap] |
rs17442297 | 1.00[JPT][hapmap] |
rs17442742 | 1.00[JPT][hapmap] |
rs17442924 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs17442980 | 1.00[JPT][hapmap] |
rs17443078 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs17443185 | 1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs17443206 | 1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs17443366 | 1.00[JPT][hapmap] |
rs17443380 | 1.00[JPT][hapmap] |
rs17443387 | 1.00[JPT][hapmap] |
rs17443504 | 1.00[JPT][hapmap] |
rs17443882 | 1.00[JPT][hapmap] |
rs17443909 | 0.80[EUR][1000 genomes] |
rs17443916 | 1.00[JPT][hapmap] |
rs17443951 | 1.00[JPT][hapmap] |
rs17444021 | 1.00[JPT][hapmap] |
rs17444033 | 1.00[JPT][hapmap] |
rs17444299 | 1.00[JPT][hapmap] |
rs17458093 | 1.00[JPT][hapmap] |
rs17458121 | 1.00[JPT][hapmap] |
rs17458202 | 1.00[JPT][hapmap] |
rs17458396 | 1.00[JPT][hapmap] |
rs17458417 | 1.00[JPT][hapmap] |
rs17458487 | 1.00[JPT][hapmap] |
rs17458528 | 1.00[JPT][hapmap] |
rs17458549 | 0.86[EUR][1000 genomes] |
rs17458808 | 0.86[EUR][1000 genomes] |
rs17458836 | 1.00[JPT][hapmap] |
rs17461337 | 1.00[JPT][hapmap] |
rs17461575 | 0.80[EUR][1000 genomes] |
rs17465610 | 0.80[EUR][1000 genomes] |
rs17465737 | 1.00[JPT][hapmap] |
rs17465751 | 1.00[JPT][hapmap] |
rs17465807 | 1.00[JPT][hapmap] |
rs17465877 | 1.00[JPT][hapmap] |
rs17465946 | 0.80[EUR][1000 genomes] |
rs17466002 | 1.00[JPT][hapmap] |
rs17466143 | 1.00[JPT][hapmap] |
rs17466206 | 1.00[JPT][hapmap] |
rs17466213 | 1.00[JPT][hapmap] |
rs17466241 | 1.00[JPT][hapmap] |
rs17466458 | 1.00[JPT][hapmap] |
rs17466514 | 1.00[JPT][hapmap] |
rs17466535 | 1.00[JPT][hapmap] |
rs17466584 | 1.00[JPT][hapmap] |
rs17466612 | 1.00[JPT][hapmap] |
rs17483857 | 1.00[JPT][hapmap] |
rs17483996 | 1.00[JPT][hapmap] |
rs17484003 | 0.86[EUR][1000 genomes] |
rs17484176 | 1.00[JPT][hapmap] |
rs17489170 | 1.00[JPT][hapmap] |
rs17489218 | 1.00[JPT][hapmap] |
rs17489225 | 1.00[JPT][hapmap] |
rs17489246 | 1.00[JPT][hapmap] |
rs17489253 | 1.00[JPT][hapmap] |
rs17489267 | 1.00[JPT][hapmap] |
rs17489365 | 1.00[JPT][hapmap] |
rs17489410 | 1.00[JPT][hapmap] |
rs17489417 | 1.00[JPT][hapmap] |
rs17489466 | 1.00[JPT][hapmap] |
rs17489501 | 1.00[JPT][hapmap] |
rs17489583 | 1.00[JPT][hapmap] |
rs17489590 | 1.00[JPT][hapmap] |
rs17489597 | 1.00[JPT][hapmap] |
rs17489638 | 1.00[JPT][hapmap] |
rs17489869 | 1.00[JPT][hapmap] |
rs17490006 | 1.00[JPT][hapmap] |
rs17490334 | 1.00[JPT][hapmap] |
rs17490341 | 1.00[JPT][hapmap] |
rs17490599 | 1.00[JPT][hapmap] |
rs17490769 | 1.00[JPT][hapmap] |
rs17490796 | 1.00[JPT][hapmap] |
rs17490810 | 1.00[JPT][hapmap] |
rs17491047 | 1.00[JPT][hapmap] |
rs17491061 | 1.00[JPT][hapmap] |
rs17491068 | 1.00[JPT][hapmap] |
rs17491180 | 1.00[JPT][hapmap] |
rs17491340 | 1.00[JPT][hapmap] |
rs17491445 | 1.00[JPT][hapmap] |
rs17491515 | 1.00[JPT][hapmap] |
rs17491529 | 1.00[JPT][hapmap] |
rs17491638 | 1.00[JPT][hapmap] |
rs17491807 | 1.00[JPT][hapmap] |
rs17491835 | 1.00[JPT][hapmap] |
rs17491863 | 1.00[JPT][hapmap] |
rs17518057 | 1.00[JPT][hapmap] |
rs17518071 | 1.00[JPT][hapmap] |
rs17518141 | 1.00[JPT][hapmap] |
rs17518148 | 1.00[JPT][hapmap] |
rs17518155 | 1.00[JPT][hapmap] |
rs17518204 | 1.00[JPT][hapmap] |
rs17518232 | 1.00[JPT][hapmap] |
rs17518343 | 1.00[JPT][hapmap] |
rs17518413 | 1.00[JPT][hapmap] |
rs17518420 | 1.00[JPT][hapmap] |
rs17518532 | 1.00[JPT][hapmap] |
rs17518910 | 1.00[JPT][hapmap] |
rs17519531 | 1.00[JPT][hapmap] |
rs17519566 | 1.00[JPT][hapmap] |
rs17519580 | 1.00[JPT][hapmap] |
rs17519615 | 1.00[JPT][hapmap] |
rs17519671 | 1.00[JPT][hapmap] |
rs17519811 | 1.00[JPT][hapmap] |
rs17519825 | 1.00[JPT][hapmap] |
rs17519832 | 1.00[JPT][hapmap] |
rs17519985 | 1.00[JPT][hapmap] |
rs17520020 | 1.00[JPT][hapmap] |
rs17520278 | 1.00[JPT][hapmap] |
rs17520292 | 1.00[JPT][hapmap] |
rs17520515 | 1.00[JPT][hapmap] |
rs17520620 | 1.00[JPT][hapmap] |
rs2638223 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2708460 | 0.93[EUR][1000 genomes] |
rs28365169 | 0.86[EUR][1000 genomes] |
rs28365173 | 0.86[EUR][1000 genomes] |
rs28365178 | 1.00[JPT][hapmap] |
rs28365191 | 1.00[JPT][hapmap] |
rs28365203 | 1.00[JPT][hapmap] |
rs28365211 | 1.00[JPT][hapmap] |
rs28365221 | 1.00[JPT][hapmap] |
rs28365226 | 1.00[JPT][hapmap] |
rs28365233 | 1.00[JPT][hapmap] |
rs28365682 | 1.00[JPT][hapmap] |
rs28365689 | 0.86[EUR][1000 genomes] |
rs28365690 | 1.00[JPT][hapmap] |
rs28370643 | 1.00[JPT][hapmap] |
rs28370649 | 1.00[JPT][hapmap];0.86[EUR][1000 genomes] |
rs28370650 | 0.86[EUR][1000 genomes] |
rs28370652 | 1.00[JPT][hapmap] |
rs28370655 | 1.00[JPT][hapmap] |
rs28370658 | 1.00[JPT][hapmap] |
rs28370665 | 1.00[JPT][hapmap] |
rs28370670 | 1.00[JPT][hapmap] |
rs28370672 | 1.00[JPT][hapmap] |
rs28370673 | 1.00[JPT][hapmap] |
rs28370682 | 1.00[JPT][hapmap];0.80[EUR][1000 genomes] |
rs28370750 | 1.00[JPT][hapmap] |
rs28370751 | 1.00[JPT][hapmap] |
rs28370755 | 1.00[JPT][hapmap] |
rs28370764 | 1.00[JPT][hapmap] |
rs28370765 | 1.00[JPT][hapmap] |
rs28370767 | 1.00[JPT][hapmap] |
rs28370768 | 1.00[JPT][hapmap] |
rs28370771 | 1.00[JPT][hapmap] |
rs28370772 | 1.00[JPT][hapmap] |
rs28370776 | 1.00[JPT][hapmap] |
rs28370779 | 1.00[JPT][hapmap] |
rs28370787 | 1.00[JPT][hapmap] |
rs28370793 | 1.00[JPT][hapmap] |
rs28370796 | 1.00[JPT][hapmap] |
rs28370818 | 1.00[JPT][hapmap] |
rs28370823 | 1.00[JPT][hapmap] |
rs28370826 | 1.00[JPT][hapmap] |
rs28370830 | 0.80[EUR][1000 genomes] |
rs4767965 | 0.80[EUR][1000 genomes] |
rs4768213 | 0.86[EUR][1000 genomes] |
rs72547977 | 0.80[EUR][1000 genomes] |
rs729215 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv558596 | chr12:40413698-40591117 | Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv1045516 | chr12:40543200-40589557 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | n/a |
3 | nsv1044685 | chr12:40574460-40771612 | Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:40585600-40587200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
2 | chr12:40585800-40587000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
3 | chr12:40585800-40587200 | Enhancers | HUES48 Cell Line | embryonic stem cell |
4 | chr12:40585800-40587400 | Enhancers | HUES64 Cell Line | embryonic stem cell |
5 | chr12:40586000-40586200 | Enhancers | GM12878-XiMat | blood |
6 | chr12:40586000-40586400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
7 | chr12:40586000-40586800 | Enhancers | Primary B cells from cord blood | blood |
8 | chr12:40586000-40586800 | Enhancers | Primary B cells from peripheral blood | blood |
9 | chr12:40586000-40587000 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
10 | chr12:40586000-40587000 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
11 | chr12:40586000-40587400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
12 | chr12:40586000-40587600 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
13 | chr12:40586000-40591000 | Enhancers | Primary neutrophils fromperipheralblood | blood |