Variant report
Variant | rs66473061 |
---|---|
Chromosome Location | chr7:120124873-120124874 |
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 | chr7:120115577..120117354-chr7:120124597..120127119,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10085878 | 0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10230753 | 0.88[EUR][1000 genomes] |
rs10233829 | 0.93[ASN][1000 genomes] |
rs10245507 | 0.92[ASN][1000 genomes] |
rs10258480 | 0.81[ASN][1000 genomes] |
rs10274789 | 0.92[ASN][1000 genomes] |
rs10275068 | 0.93[ASN][1000 genomes] |
rs10276390 | 0.91[ASN][1000 genomes] |
rs10279267 | 0.82[ASN][1000 genomes] |
rs10279812 | 0.92[ASN][1000 genomes] |
rs1029978 | 0.92[ASN][1000 genomes] |
rs10488298 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10488299 | 0.92[ASN][1000 genomes] |
rs10953913 | 0.82[AMR][1000 genomes] |
rs10953918 | 0.92[ASN][1000 genomes] |
rs11761401 | 0.92[ASN][1000 genomes] |
rs11980474 | 0.80[ASN][1000 genomes] |
rs12531042 | 0.91[ASN][1000 genomes] |
rs12531730 | 0.92[ASN][1000 genomes] |
rs12536754 | 0.93[ASN][1000 genomes] |
rs12537274 | 0.80[ASN][1000 genomes] |
rs12666810 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1358369 | 0.80[ASN][1000 genomes] |
rs1405836 | 0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1527651 | 0.88[EUR][1000 genomes] |
rs1527652 | 0.88[EUR][1000 genomes] |
rs1527653 | 0.88[EUR][1000 genomes] |
rs17132703 | 0.92[ASN][1000 genomes] |
rs17142724 | 0.82[AMR][1000 genomes] |
rs1881023 | 0.88[EUR][1000 genomes] |
rs1881024 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1997229 | 0.88[EUR][1000 genomes] |
rs2041679 | 0.92[ASN][1000 genomes] |
rs2041680 | 0.92[ASN][1000 genomes] |
rs4464900 | 0.88[EUR][1000 genomes] |
rs4610678 | 0.88[EUR][1000 genomes] |
rs4730963 | 0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs58738977 | 0.92[ASN][1000 genomes] |
rs59732893 | 0.92[ASN][1000 genomes] |
rs62473168 | 0.92[ASN][1000 genomes] |
rs6466748 | 0.93[ASN][1000 genomes] |
rs6466752 | 0.88[EUR][1000 genomes] |
rs66597280 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs67181710 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs67430445 | 0.82[AMR][1000 genomes] |
rs67560031 | 0.82[AMR][1000 genomes] |
rs68060610 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6948806 | 0.92[ASN][1000 genomes] |
rs6951226 | 0.88[EUR][1000 genomes] |
rs6966670 | 0.92[ASN][1000 genomes] |
rs702414 | 0.80[ASN][1000 genomes] |
rs702415 | 0.85[ASN][1000 genomes] |
rs702416 | 0.83[ASN][1000 genomes] |
rs723908 | 0.91[ASN][1000 genomes] |
rs7781883 | 0.88[EUR][1000 genomes] |
rs7785421 | 0.91[ASN][1000 genomes] |
rs7785571 | 0.81[ASN][1000 genomes] |
rs7788666 | 0.92[ASN][1000 genomes] |
rs7798075 | 0.93[ASN][1000 genomes] |
rs7808260 | 0.88[EUR][1000 genomes] |
rs7809573 | 0.92[ASN][1000 genomes] |
rs802332 | 0.85[ASN][1000 genomes] |
rs802333 | 0.84[ASN][1000 genomes] |
rs802334 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802335 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802336 | 0.84[ASN][1000 genomes] |
rs802337 | 0.84[ASN][1000 genomes] |
rs802338 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802339 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802344 | 0.91[ASN][1000 genomes] |
rs802345 | 0.91[ASN][1000 genomes] |
rs802346 | 0.80[ASN][1000 genomes] |
rs802347 | 0.91[ASN][1000 genomes] |
rs802348 | 0.80[ASN][1000 genomes] |
rs802349 | 0.80[ASN][1000 genomes] |
rs802350 | 0.90[ASN][1000 genomes] |
rs802351 | 0.80[ASN][1000 genomes] |
rs802352 | 0.80[ASN][1000 genomes] |
rs802353 | 0.80[ASN][1000 genomes] |
rs802354 | 0.91[ASN][1000 genomes] |
rs802355 | 0.80[ASN][1000 genomes] |
rs802356 | 0.91[ASN][1000 genomes] |
rs802357 | 0.91[ASN][1000 genomes] |
rs802358 | 0.80[ASN][1000 genomes] |
rs802359 | 0.91[ASN][1000 genomes] |
rs802362 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802363 | 0.84[ASN][1000 genomes] |
rs802364 | 0.84[ASN][1000 genomes] |
rs802365 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802367 | 0.84[ASN][1000 genomes] |
rs802368 | 0.82[ASN][1000 genomes] |
rs802369 | 0.84[ASN][1000 genomes] |
rs802370 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802371 | 0.84[ASN][1000 genomes] |
rs802372 | 0.84[ASN][1000 genomes] |
rs802373 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802374 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802376 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802377 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs802378 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9641639 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9641640 | 0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv516686 | chr7:120015843-120223084 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv1026821 | chr7:120020317-120190437 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv889116 | chr7:120098304-120180671 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv889117 | chr7:120122040-120266458 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:120117400-120126400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr7:120119200-120126200 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
3 | chr7:120119600-120126200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
4 | chr7:120119800-120126200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
5 | chr7:120121200-120131200 | Weak transcription | GM12878-XiMat | blood |
6 | chr7:120122600-120139400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |