Variant report
Variant | rs72898898 |
---|---|
Chromosome Location | chr2:189492783-189492784 |
allele | G/T |
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 | chr2:189492002..189493869-chr2:189841619..189843141,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000221502 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10931357 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs10931368 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11674580 | 1.00[AFR][1000 genomes] |
rs11676244 | 1.00[AFR][1000 genomes] |
rs11676569 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11678035 | 1.00[AFR][1000 genomes] |
rs11678718 | 1.00[AFR][1000 genomes] |
rs11679949 | 0.86[EUR][1000 genomes] |
rs11681365 | 1.00[AFR][1000 genomes] |
rs11682895 | 1.00[AFR][1000 genomes] |
rs11683909 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs11683969 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs11684224 | 1.00[AFR][1000 genomes] |
rs11685643 | 0.86[EUR][1000 genomes] |
rs11687872 | 1.00[AFR][1000 genomes] |
rs11688482 | 1.00[AFR][1000 genomes] |
rs11692432 | 1.00[ASN][1000 genomes] |
rs11693105 | 0.86[EUR][1000 genomes] |
rs11695177 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs11695250 | 1.00[AFR][1000 genomes] |
rs11695327 | 1.00[AFR][1000 genomes] |
rs12151605 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs34323074 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs34587834 | 1.00[AFR][1000 genomes] |
rs57067423 | 0.86[EUR][1000 genomes] |
rs57210291 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs57351486 | 1.00[AFR][1000 genomes] |
rs58210062 | 1.00[AFR][1000 genomes] |
rs59668663 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs60162413 | 1.00[AFR][1000 genomes] |
rs60307701 | 1.00[AFR][1000 genomes] |
rs60514585 | 1.00[AFR][1000 genomes] |
rs60602630 | 1.00[AFR][1000 genomes] |
rs60608780 | 1.00[AFR][1000 genomes] |
rs60894296 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60916684 | 1.00[AFR][1000 genomes] |
rs61011178 | 1.00[AFR][1000 genomes] |
rs61500341 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72896824 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72896833 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72896844 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72896851 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72896856 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72896869 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72896876 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72896879 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72896898 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898830 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898840 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898843 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898858 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898866 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898876 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898887 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72898900 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900830 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72900842 | 1.00[EUR][1000 genomes] |
rs72900845 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900848 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900849 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900852 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900854 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72900855 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72900857 | 0.86[EUR][1000 genomes] |
rs72900861 | 0.86[EUR][1000 genomes] |
rs72900862 | 1.00[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs72900870 | 1.00[AFR][1000 genomes] |
rs72902608 | 1.00[AFR][1000 genomes] |
rs72902633 | 1.00[AFR][1000 genomes] |
rs72902639 | 1.00[AFR][1000 genomes] |
rs72902642 | 1.00[AFR][1000 genomes] |
rs72902649 | 1.00[AFR][1000 genomes] |
rs72902655 | 1.00[AFR][1000 genomes] |
rs72902678 | 1.00[AFR][1000 genomes] |
rs72902691 | 1.00[AFR][1000 genomes] |
rs72904650 | 1.00[AFR][1000 genomes] |
rs72904664 | 1.00[AFR][1000 genomes] |
rs72904665 | 1.00[AFR][1000 genomes] |
rs72904686 | 1.00[AFR][1000 genomes] |
rs72904690 | 1.00[AFR][1000 genomes] |
rs72904691 | 1.00[AFR][1000 genomes] |
rs72904696 | 1.00[AFR][1000 genomes] |
rs72904698 | 1.00[AFR][1000 genomes] |
rs72904699 | 1.00[AFR][1000 genomes] |
rs72904701 | 1.00[AFR][1000 genomes] |
rs72904702 | 1.00[AFR][1000 genomes] |
rs72906605 | 1.00[AFR][1000 genomes] |
rs72906610 | 1.00[AFR][1000 genomes] |
rs72906611 | 1.00[AFR][1000 genomes] |
rs72906620 | 1.00[AFR][1000 genomes] |
rs72906621 | 1.00[AFR][1000 genomes] |
rs72906633 | 1.00[AFR][1000 genomes] |
rs72906638 | 1.00[AFR][1000 genomes] |
rs72906640 | 1.00[AFR][1000 genomes] |
rs72906643 | 1.00[AFR][1000 genomes] |
rs72906655 | 1.00[AFR][1000 genomes] |
rs72906657 | 1.00[AFR][1000 genomes] |
rs72906662 | 1.00[AFR][1000 genomes] |
rs72906664 | 1.00[AFR][1000 genomes] |
rs72906691 | 1.00[AFR][1000 genomes] |
rs72906692 | 1.00[AFR][1000 genomes] |
rs72906695 | 1.00[AFR][1000 genomes] |
rs72906698 | 1.00[AFR][1000 genomes] |
rs72909566 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909568 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909571 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909573 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909575 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909576 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909577 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909579 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909590 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909594 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909595 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72909598 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911406 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911432 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911439 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911445 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911448 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911463 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911465 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911476 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911497 | 0.86[EUR][1000 genomes] |
rs72911499 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72911501 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72913327 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72913360 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs72913365 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs7423329 | 0.80[EUR][1000 genomes] |
rs7579593 | 0.86[EUR][1000 genomes] |
rs7579655 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv584055 | chr2:189266823-189493686 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
2 | nsv834489 | chr2:189329027-189494224 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1003974 | chr2:189331760-189827814 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:189484800-189494600 | Weak transcription | Aorta | Aorta |
2 | chr2:189488200-189494000 | Weak transcription | Fetal Stomach | stomach |
3 | chr2:189489200-189494000 | Weak transcription | NH-A | brain |
4 | chr2:189489400-189493400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
5 | chr2:189489400-189494000 | Weak transcription | NHLF | lung |
6 | chr2:189489400-189494200 | Weak transcription | Muscle Satellite Cultured Cells | -- |
7 | chr2:189489400-189494400 | Weak transcription | Fetal Lung | lung |
8 | chr2:189489800-189493200 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
9 | chr2:189489800-189493400 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
10 | chr2:189489800-189493800 | Weak transcription | Osteobl | bone |
11 | chr2:189490000-189493200 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
12 | chr2:189492000-189496600 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
13 | chr2:189492200-189493200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
14 | chr2:189492400-189495400 | Enhancers | NHDF-Ad | bronchial |
15 | chr2:189492600-189493200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |