Variant report
Variant | rs11770322 |
---|---|
Chromosome Location | chr7:33295491-33295492 |
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 | chr7:33283153..33284693-chr7:33295167..33297777,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10224956 | 0.88[AMR][1000 genomes] |
rs10227739 | 0.89[AMR][1000 genomes] |
rs10232564 | 0.88[AMR][1000 genomes] |
rs10233642 | 0.88[AMR][1000 genomes] |
rs10233793 | 0.86[AMR][1000 genomes] |
rs10236927 | 0.88[AMR][1000 genomes] |
rs10237088 | 0.88[AMR][1000 genomes] |
rs10240165 | 0.88[AMR][1000 genomes] |
rs10240664 | 0.96[AMR][1000 genomes] |
rs10241188 | 0.90[AMR][1000 genomes] |
rs10255689 | 0.88[AMR][1000 genomes] |
rs10260593 | 0.86[AMR][1000 genomes] |
rs10261756 | 0.91[AMR][1000 genomes] |
rs10262228 | 0.96[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs10269937 | 0.88[AMR][1000 genomes] |
rs10270961 | 0.88[AMR][1000 genomes] |
rs10272214 | 0.96[AMR][1000 genomes] |
rs10272253 | 0.90[AMR][1000 genomes] |
rs10278228 | 0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10951376 | 0.88[AMR][1000 genomes] |
rs10951377 | 0.93[AMR][1000 genomes] |
rs10951380 | 0.98[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10951381 | 0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs11760829 | 0.88[AMR][1000 genomes] |
rs11760830 | 0.91[AMR][1000 genomes] |
rs11763306 | 0.88[AMR][1000 genomes] |
rs11765727 | 0.82[EUR][1000 genomes] |
rs11766506 | 0.88[AMR][1000 genomes] |
rs11766521 | 0.88[AMR][1000 genomes] |
rs11768050 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11769811 | 0.88[AMR][1000 genomes] |
rs11771086 | 0.82[EUR][1000 genomes] |
rs11772401 | 0.91[AMR][1000 genomes] |
rs11978733 | 0.82[EUR][1000 genomes] |
rs11982544 | 0.82[EUR][1000 genomes] |
rs12056065 | 0.82[EUR][1000 genomes] |
rs12666753 | 1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12669713 | 0.88[AMR][1000 genomes] |
rs12671396 | 0.89[AMR][1000 genomes] |
rs12673026 | 0.88[AMR][1000 genomes] |
rs12674040 | 0.88[AMR][1000 genomes] |
rs12674454 | 0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12701275 | 0.88[AMR][1000 genomes] |
rs12701285 | 0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12701289 | 0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1304294 | 0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs13224392 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13224684 | 0.93[AMR][1000 genomes] |
rs13225836 | 0.91[AMR][1000 genomes] |
rs13227275 | 0.88[AMR][1000 genomes] |
rs13228512 | 0.88[AMR][1000 genomes] |
rs13231353 | 0.88[AMR][1000 genomes] |
rs13233383 | 0.91[AMR][1000 genomes] |
rs13233431 | 0.93[AMR][1000 genomes] |
rs13236414 | 0.88[AMR][1000 genomes] |
rs13236865 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13238407 | 0.82[EUR][1000 genomes] |
rs13240884 | 0.86[AMR][1000 genomes] |
rs13244450 | 0.88[AMR][1000 genomes] |
rs1362367 | 0.88[AMR][1000 genomes] |
rs1406606 | 0.88[AMR][1000 genomes] |
rs1468797 | 0.89[AMR][1000 genomes] |
rs1548879 | 0.88[AMR][1000 genomes] |
rs1569239 | 0.88[AMR][1000 genomes] |
rs17150810 | 0.96[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs17169835 | 0.88[AMR][1000 genomes] |
rs17169840 | 0.88[AMR][1000 genomes] |
rs17169847 | 0.88[AMR][1000 genomes] |
rs17169855 | 0.88[AMR][1000 genomes] |
rs17169881 | 0.88[AMR][1000 genomes] |
rs17169913 | 0.93[AMR][1000 genomes] |
rs17170142 | 0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17170174 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs17170175 | 0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1861298 | 0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2160253 | 0.96[AMR][1000 genomes] |
rs2178343 | 0.88[AMR][1000 genomes] |
rs28714260 | 0.88[AMR][1000 genomes] |
rs28764825 | 0.93[AMR][1000 genomes] |
rs28778101 | 0.88[AMR][1000 genomes] |
rs28825171 | 0.88[AMR][1000 genomes] |
rs34171272 | 0.91[AMR][1000 genomes] |
rs34213032 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs34262563 | 0.91[AMR][1000 genomes] |
rs34493378 | 0.98[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs34506512 | 0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs34540469 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35067143 | 0.82[EUR][1000 genomes] |
rs35195868 | 0.88[AMR][1000 genomes] |
rs35543773 | 0.88[AMR][1000 genomes] |
rs35665200 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36081731 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs36192455 | 0.88[AMR][1000 genomes] |
rs3750123 | 0.88[AMR][1000 genomes] |
rs4720103 | 0.88[AMR][1000 genomes] |
rs4720104 | 0.88[AMR][1000 genomes] |
rs4720105 | 0.88[AMR][1000 genomes] |
rs4720106 | 0.86[AMR][1000 genomes] |
rs4720107 | 0.88[AMR][1000 genomes] |
rs4723254 | 0.88[AMR][1000 genomes] |
rs4723255 | 0.88[AMR][1000 genomes] |
rs4723256 | 0.88[AMR][1000 genomes] |
rs4723258 | 0.88[AMR][1000 genomes] |
rs4723259 | 0.88[AMR][1000 genomes] |
rs4723260 | 0.85[AMR][1000 genomes] |
rs4723262 | 0.88[AMR][1000 genomes] |
rs4723266 | 0.88[AMR][1000 genomes] |
rs4723278 | 0.82[EUR][1000 genomes] |
rs4723279 | 0.82[EUR][1000 genomes] |
rs59311005 | 0.88[AMR][1000 genomes] |
rs60115200 | 0.88[AMR][1000 genomes] |
rs6952877 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6953193 | 0.93[AMR][1000 genomes] |
rs6953313 | 0.88[AMR][1000 genomes] |
rs6953348 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6956981 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6970226 | 0.88[AMR][1000 genomes] |
rs6973757 | 0.91[AMR][1000 genomes] |
rs6978749 | 0.88[AMR][1000 genomes] |
rs71532562 | 0.88[AMR][1000 genomes] |
rs71532563 | 0.84[AMR][1000 genomes] |
rs71532565 | 0.88[AMR][1000 genomes] |
rs71532573 | 0.82[EUR][1000 genomes] |
rs71534347 | 0.86[AMR][1000 genomes] |
rs71534348 | 0.98[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs7457370 | 0.91[AMR][1000 genomes] |
rs764127 | 0.88[AMR][1000 genomes] |
rs7777101 | 0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7783612 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7784516 | 0.88[AMR][1000 genomes] |
rs7784540 | 0.88[AMR][1000 genomes] |
rs7784815 | 0.88[AMR][1000 genomes] |
rs7804742 | 0.88[AMR][1000 genomes] |
rs7810388 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9638888 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9638889 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9791864 | 0.93[AMR][1000 genomes] |
rs986554 | 0.96[AMR][1000 genomes] |
rs987501 | 0.93[AMR][1000 genomes] |
rs9886317 | 0.88[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830943 | chr7:33167106-33352759 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 7 gene(s) | inside rSNPs | diseases |
2 | nsv606610 | chr7:33218763-33486316 | Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1016416 | chr7:33241443-33559477 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv916660 | chr7:33272493-33506384 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:33283800-33316000 | Weak transcription | Ovary | ovary |
2 | chr7:33287200-33296000 | Weak transcription | Pancreas | Pancrea |
3 | chr7:33288800-33317600 | Weak transcription | Gastric | stomach |
4 | chr7:33289400-33309000 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
5 | chr7:33289600-33310800 | Weak transcription | Psoas Muscle | Psoas |
6 | chr7:33290000-33316200 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
7 | chr7:33290800-33295800 | Weak transcription | Fetal Lung | lung |
8 | chr7:33290800-33309000 | Weak transcription | Fetal Stomach | stomach |
9 | chr7:33290800-33316400 | Weak transcription | Aorta | Aorta |
10 | chr7:33291200-33297600 | Weak transcription | Osteobl | bone |
11 | chr7:33291200-33297800 | Weak transcription | Colon Smooth Muscle | Colon |
12 | chr7:33291200-33298000 | Weak transcription | NHDF-Ad | bronchial |
13 | chr7:33291200-33316000 | Weak transcription | Primary T cells from cord blood | blood |
14 | chr7:33291600-33305200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
15 | chr7:33291800-33307600 | Weak transcription | Left Ventricle | heart |
16 | chr7:33293400-33302200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
17 | chr7:33295400-33299800 | Weak transcription | HepG2 | liver |