Variant report
Variant | rs1893807 |
---|---|
Chromosome Location | chr11:100927282-100927283 |
allele | A/G |
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 | chr11:100926600..100927336-chr11:101206798..101207521,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10895056 | 0.80[ASN][1000 genomes] |
rs10895058 | 0.83[ASN][1000 genomes] |
rs10895063 | 0.86[ASN][1000 genomes] |
rs10895065 | 0.84[ASN][1000 genomes] |
rs11224580 | 0.83[ASN][1000 genomes] |
rs11224589 | 0.86[ASN][1000 genomes] |
rs11224592 | 0.86[ASN][1000 genomes] |
rs11224593 | 0.86[ASN][1000 genomes] |
rs11224594 | 0.84[ASN][1000 genomes] |
rs11224598 | 0.85[ASN][1000 genomes] |
rs11224599 | 0.80[ASN][1000 genomes] |
rs1144133 | 0.99[ASN][1000 genomes] |
rs1145455 | 0.84[ASN][1000 genomes] |
rs1145464 | 0.88[ASN][1000 genomes] |
rs11571159 | 0.81[ASN][1000 genomes] |
rs11571171 | 0.87[ASN][1000 genomes] |
rs1217845 | 0.93[ASN][1000 genomes] |
rs1217860 | 0.86[ASN][1000 genomes] |
rs1302679 | 0.90[ASN][1000 genomes] |
rs1303052 | 0.88[ASN][1000 genomes] |
rs1456764 | 0.84[ASN][1000 genomes] |
rs1456765 | 0.84[ASN][1000 genomes] |
rs1824126 | 0.85[ASN][1000 genomes] |
rs1824127 | 0.86[ASN][1000 genomes] |
rs474640 | 0.84[ASN][1000 genomes] |
rs475902 | 0.81[ASN][1000 genomes] |
rs477266 | 0.84[ASN][1000 genomes] |
rs481495 | 0.84[ASN][1000 genomes] |
rs481855 | 0.88[ASN][1000 genomes] |
rs481883 | 0.84[ASN][1000 genomes] |
rs483376 | 0.84[ASN][1000 genomes] |
rs483493 | 0.85[ASN][1000 genomes] |
rs483678 | 0.88[ASN][1000 genomes] |
rs485506 | 0.88[ASN][1000 genomes] |
rs486960 | 0.84[ASN][1000 genomes] |
rs487271 | 0.88[ASN][1000 genomes] |
rs488080 | 0.84[ASN][1000 genomes] |
rs489034 | 0.90[ASN][1000 genomes] |
rs491722 | 0.82[ASN][1000 genomes] |
rs491893 | 0.83[ASN][1000 genomes] |
rs492599 | 0.84[ASN][1000 genomes] |
rs493508 | 0.84[ASN][1000 genomes] |
rs494424 | 0.88[ASN][1000 genomes] |
rs495384 | 0.81[ASN][1000 genomes] |
rs495391 | 0.81[ASN][1000 genomes] |
rs496208 | 0.81[ASN][1000 genomes] |
rs498101 | 0.81[ASN][1000 genomes] |
rs499664 | 0.90[ASN][1000 genomes] |
rs503602 | 0.93[ASN][1000 genomes] |
rs506045 | 0.84[ASN][1000 genomes] |
rs506092 | 0.86[ASN][1000 genomes] |
rs507044 | 0.88[ASN][1000 genomes] |
rs508120 | 0.88[ASN][1000 genomes] |
rs508533 | 0.81[ASN][1000 genomes] |
rs508653 | 0.86[ASN][1000 genomes] |
rs511298 | 0.93[ASN][1000 genomes] |
rs513081 | 0.86[ASN][1000 genomes] |
rs515059 | 0.88[ASN][1000 genomes] |
rs516693 | 0.86[ASN][1000 genomes] |
rs517930 | 0.84[ASN][1000 genomes] |
rs518382 | 0.82[ASN][1000 genomes] |
rs519220 | 0.83[ASN][1000 genomes] |
rs521028 | 0.90[ASN][1000 genomes] |
rs521744 | 0.81[ASN][1000 genomes] |
rs522053 | 0.85[ASN][1000 genomes] |
rs523323 | 0.86[ASN][1000 genomes] |
rs528673 | 0.81[ASN][1000 genomes] |
rs529775 | 0.86[ASN][1000 genomes] |
rs531666 | 0.88[ASN][1000 genomes] |
rs537120 | 0.84[ASN][1000 genomes] |
rs538168 | 0.84[ASN][1000 genomes] |
rs538915 | 0.88[ASN][1000 genomes] |
rs540622 | 0.82[ASN][1000 genomes] |
rs540763 | 0.84[ASN][1000 genomes] |
rs542384 | 0.81[ASN][1000 genomes] |
rs543215 | 0.80[ASN][1000 genomes] |
rs545838 | 0.83[ASN][1000 genomes] |
rs546289 | 0.83[ASN][1000 genomes] |
rs547378 | 0.82[ASN][1000 genomes] |
rs547565 | 0.99[ASN][1000 genomes] |
rs550382 | 0.82[ASN][1000 genomes] |
rs550468 | 0.93[ASN][1000 genomes] |
rs553272 | 0.85[ASN][1000 genomes] |
rs554101 | 0.85[ASN][1000 genomes] |
rs555653 | 0.84[ASN][1000 genomes] |
rs556238 | 0.81[ASN][1000 genomes] |
rs557052 | 0.81[ASN][1000 genomes] |
rs560527 | 0.83[ASN][1000 genomes] |
rs561511 | 0.84[ASN][1000 genomes] |
rs561572 | 0.84[ASN][1000 genomes] |
rs561650 | 0.97[ASN][1000 genomes] |
rs562764 | 0.83[ASN][1000 genomes] |
rs564419 | 0.84[ASN][1000 genomes] |
rs566761 | 0.84[ASN][1000 genomes] |
rs569723 | 0.84[ASN][1000 genomes] |
rs569857 | 0.99[ASN][1000 genomes] |
rs569938 | 0.81[ASN][1000 genomes] |
rs570078 | 0.83[ASN][1000 genomes] |
rs572483 | 0.88[ASN][1000 genomes] |
rs572775 | 0.90[ASN][1000 genomes] |
rs573094 | 0.81[ASN][1000 genomes] |
rs573096 | 0.82[ASN][1000 genomes] |
rs578938 | 0.88[ASN][1000 genomes] |
rs587955 | 0.90[ASN][1000 genomes] |
rs590688 | 0.83[ASN][1000 genomes] |
rs600678 | 0.84[ASN][1000 genomes] |
rs600692 | 0.84[ASN][1000 genomes] |
rs600837 | 0.86[ASN][1000 genomes] |
rs601046 | 0.82[ASN][1000 genomes] |
rs618032 | 0.81[ASN][1000 genomes] |
rs618972 | 0.97[ASN][1000 genomes] |
rs634179 | 0.86[ASN][1000 genomes] |
rs635984 | 0.82[ASN][1000 genomes] |
rs645213 | 0.82[ASN][1000 genomes] |
rs647420 | 0.81[ASN][1000 genomes] |
rs648838 | 0.84[ASN][1000 genomes] |
rs651977 | 0.83[ASN][1000 genomes] |
rs653752 | 0.83[ASN][1000 genomes] |
rs657516 | 0.99[ASN][1000 genomes] |
rs660912 | 0.84[ASN][1000 genomes] |
rs664882 | 0.84[ASN][1000 genomes] |
rs665617 | 0.93[ASN][1000 genomes] |
rs666553 | 0.93[ASN][1000 genomes] |
rs685828 | 0.88[ASN][1000 genomes] |
rs694070 | 0.86[ASN][1000 genomes] |
rs694317 | 0.90[ASN][1000 genomes] |
rs7106686 | 0.84[ASN][1000 genomes] |
rs73573609 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1048356 | chr11:100713096-101058995 | Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | nsv541154 | chr11:100713096-101058995 | Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:100905200-100935800 | Weak transcription | Colon Smooth Muscle | Colon |
2 | chr11:100905400-100997600 | Weak transcription | Left Ventricle | heart |
3 | chr11:100914400-100935600 | Weak transcription | Aorta | Aorta |
4 | chr11:100918800-100930800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
5 | chr11:100927200-100927400 | Enhancers | Ovary | ovary |