Variant report
Variant | rs7109807 |
---|---|
Chromosome Location | chr11:55889687-55889688 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:61)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:55889658-55889708 | ProgFib | skin: | n/a |
2 | chr11:55889658-55889708 | RPTEC | kidney: | n/a |
3 | chr11:55889658-55889708 | HNPCEpiC | eye: | n/a |
4 | chr11:55889658-55889708 | AG04449 | skin: | fetal |
5 | chr11:55889658-55889708 | PFSK-1 | brain: | n/a |
6 | chr11:55889658-55889708 | HCT-116 | colon: | n/a |
7 | chr11:55889658-55889708 | H1-hESC | embryonic stem cell: | embryo |
8 | chr11:55889658-55889708 | CMK | blood: | n/a |
9 | chr11:55889658-55889708 | AG04450 | lung: | fetal |
10 | chr11:55889658-55889708 | HCM | heart: | n/a |
11 | chr11:55889658-55889708 | HEK293 | kidney: | embryo |
12 | chr11:55889658-55889708 | HRCEpiC | kidney: | n/a |
13 | chr11:55889658-55889708 | IMR90 | lung: | fetal |
14 | chr11:55889658-55889708 | HRPEpiC | eye: | n/a |
15 | chr11:55889658-55889708 | NT2-D1 | testis: | n/a |
16 | chr11:55889658-55889708 | HCPEpiC | choroid plexus: | n/a |
17 | chr11:55889658-55889708 | NB4 | blood: | n/a |
18 | chr11:55889658-55889708 | GM19239 | blood: | n/a |
19 | chr11:55889658-55889708 | NHBE | bronchial: | n/a |
20 | chr11:55889658-55889708 | PrEC | prostate: | n/a |
21 | chr11:55889658-55889708 | GM12878 | blood: | n/a |
22 | chr11:55889658-55889708 | AoSMC | blood vessel: | n/a |
23 | chr11:55889658-55889708 | ECC-1 | luminal epithelium: | n/a |
24 | chr11:55889658-55889708 | SAEC | small airway: | n/a |
25 | chr11:55889658-55889708 | HRE | kidney: | n/a |
26 | chr11:55889658-55889708 | MCF10A-Er-Src | breast: | n/a |
27 | chr11:55889658-55889708 | HCF | heart: | n/a |
28 | chr11:55889658-55889708 | HL-60 | blood: | n/a |
29 | chr11:55889658-55889708 | HMEC | breast: | n/a |
30 | chr11:55889658-55889708 | Hepatocyte | liver: | n/a |
31 | chr11:55889658-55889708 | HPAEpiC | pulmonary alveolar: | n/a |
32 | chr11:55889658-55889708 | HUVEC | blood vessel: | n/a |
33 | chr11:55889658-55889708 | T-47D | breast: | n/a |
34 | chr11:55889658-55889708 | HEEpiC | esophagus: | n/a |
35 | chr11:55889658-55889708 | AG09319 | gingival: | n/a |
36 | chr11:55889658-55889708 | Jurkat | blood: | n/a |
37 | chr11:55889658-55889708 | SKMC | muscle: | n/a |
38 | chr11:55889658-55889708 | NH-A | brain: | n/a |
39 | chr11:55889658-55889708 | SK-N-MC | brain: | n/a |
40 | chr11:55889658-55889708 | SK-N-SH_RA | brain: | n/a |
41 | chr11:55889658-55889708 | MCF-7 | breast: | n/a |
42 | chr11:55889658-55889708 | GM12891 | blood: | n/a |
43 | chr11:55889658-55889708 | GM06990 | blood: | n/a |
44 | chr11:55889658-55889708 | HIPEpiC | eye: | n/a |
45 | chr11:55889658-55889708 | AG10803 | skin: | n/a |
46 | chr11:55889658-55889708 | BJ | skin: | n/a |
47 | chr11:55889658-55889708 | HepG2 | liver: | n/a |
48 | chr11:55889658-55889708 | SK-N-SH | brain: | n/a |
49 | chr11:55889658-55889708 | Caco-2 | colon: | n/a |
50 | chr11:55889658-55889708 | K562 | blood: | n/a |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
OR5BN2P | CpG island |
OR8H3 | CpG island |
rs_ID | r2[population] |
---|---|
rs11227518 | 0.91[CEU][hapmap] |
rs12099295 | 0.89[CEU][hapmap];0.91[EUR][1000 genomes] |
rs12270268 | 0.89[CEU][hapmap] |
rs17527401 | 0.91[CEU][hapmap] |
rs17527710 | 0.89[EUR][1000 genomes] |
rs17527788 | 0.90[CEU][hapmap];0.91[EUR][1000 genomes] |
rs17527850 | 0.91[EUR][1000 genomes] |
rs17527864 | 0.91[EUR][1000 genomes] |
rs17528782 | 0.91[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17528803 | 0.91[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17530318 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17530360 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17530416 | 0.91[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17530423 | 0.91[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17531417 | 0.91[CEU][hapmap] |
rs17597589 | 0.90[CEU][hapmap] |
rs17597625 | 0.90[CEU][hapmap] |
rs17597646 | 0.89[CEU][hapmap] |
rs17598017 | 0.91[CEU][hapmap] |
rs17598045 | 0.90[CEU][hapmap] |
rs17598094 | 0.90[CEU][hapmap] |
rs17599457 | 0.91[CEU][hapmap] |
rs17599471 | 0.90[CEU][hapmap] |
rs17599899 | 0.90[CEU][hapmap];0.91[EUR][1000 genomes] |
rs17599913 | 0.91[EUR][1000 genomes] |
rs17600692 | 0.91[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17600784 | 0.91[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17600820 | 0.91[CEU][hapmap];0.94[EUR][1000 genomes] |
rs17600939 | 0.90[CEU][hapmap] |
rs17601361 | 0.91[CEU][hapmap] |
rs17601459 | 0.90[CEU][hapmap] |
rs17603011 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17603260 | 0.91[CEU][hapmap] |
rs17610726 | 0.91[CEU][hapmap] |
rs17613345 | 0.91[CEU][hapmap] |
rs1947923 | 0.90[CEU][hapmap];0.94[EUR][1000 genomes] |
rs2170446 | 0.91[CEU][hapmap] |
rs2449138 | 0.94[EUR][1000 genomes] |
rs2512932 | 0.94[EUR][1000 genomes] |
rs2512961 | 0.90[CEU][hapmap] |
rs28421520 | 1.00[EUR][1000 genomes] |
rs28537497 | 1.00[EUR][1000 genomes] |
rs28688517 | 1.00[EUR][1000 genomes] |
rs2870138 | 0.91[CEU][hapmap] |
rs4338547 | 0.91[CEU][hapmap] |
rs55696205 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55833459 | 0.91[EUR][1000 genomes] |
rs56057397 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs56149224 | 0.86[AMR][1000 genomes] |
rs56176720 | 0.91[EUR][1000 genomes] |
rs56178210 | 0.91[EUR][1000 genomes] |
rs56208265 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56301431 | 0.91[EUR][1000 genomes] |
rs56370444 | 0.91[EUR][1000 genomes] |
rs56393785 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56402650 | 0.89[EUR][1000 genomes] |
rs61746167 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887074 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887088 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887089 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887090 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887091 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887092 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887137 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs61887142 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61887143 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs61888282 | 1.00[AFR][1000 genomes] |
rs61888286 | 1.00[AFR][1000 genomes] |
rs61888467 | 0.87[EUR][1000 genomes] |
rs61888468 | 0.94[EUR][1000 genomes] |
rs61888469 | 0.94[EUR][1000 genomes] |
rs61888470 | 0.94[EUR][1000 genomes] |
rs61888471 | 0.94[EUR][1000 genomes] |
rs61888472 | 0.94[EUR][1000 genomes] |
rs61888473 | 0.94[EUR][1000 genomes] |
rs61888545 | 0.94[EUR][1000 genomes] |
rs61888546 | 0.94[EUR][1000 genomes] |
rs61889622 | 0.87[EUR][1000 genomes] |
rs61889973 | 0.94[EUR][1000 genomes] |
rs61889974 | 0.94[EUR][1000 genomes] |
rs61889975 | 0.94[EUR][1000 genomes] |
rs61891189 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891190 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891191 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891194 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891195 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891196 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs61891197 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891198 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891199 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891201 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891202 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891203 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891205 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891206 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891209 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs61891210 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61891211 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61896242 | 0.84[EUR][1000 genomes] |
rs61896244 | 0.91[EUR][1000 genomes] |
rs61896245 | 0.91[EUR][1000 genomes] |
rs61896247 | 0.91[EUR][1000 genomes] |
rs61896248 | 0.91[EUR][1000 genomes] |
rs61896249 | 0.91[EUR][1000 genomes] |
rs61896250 | 0.91[EUR][1000 genomes] |
rs61896251 | 0.91[EUR][1000 genomes] |
rs61896253 | 0.91[EUR][1000 genomes] |
rs61896254 | 0.91[EUR][1000 genomes] |
rs61896255 | 0.91[EUR][1000 genomes] |
rs61896256 | 0.91[EUR][1000 genomes] |
rs61896257 | 0.91[EUR][1000 genomes] |
rs61896258 | 0.91[EUR][1000 genomes] |
rs61896259 | 0.91[EUR][1000 genomes] |
rs61896960 | 0.91[EUR][1000 genomes] |
rs61896961 | 0.91[EUR][1000 genomes] |
rs61896962 | 0.91[EUR][1000 genomes] |
rs61896963 | 0.91[EUR][1000 genomes] |
rs61896964 | 0.91[EUR][1000 genomes] |
rs61896965 | 0.91[EUR][1000 genomes] |
rs61896966 | 0.91[EUR][1000 genomes] |
rs7102893 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7104912 | 0.92[EUR][1000 genomes] |
rs7109136 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7110317 | 0.90[CEU][hapmap] |
rs7110689 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7112887 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7113176 | 0.90[CEU][hapmap] |
rs7113418 | 0.90[CEU][hapmap] |
rs7113601 | 0.92[EUR][1000 genomes] |
rs7114852 | 0.91[EUR][1000 genomes] |
rs7114865 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7119253 | 0.90[CEU][hapmap] |
rs7125690 | 0.90[CEU][hapmap] |
rs7128453 | 0.94[EUR][1000 genomes] |
rs7131505 | 0.92[EUR][1000 genomes] |
rs7131616 | 0.92[EUR][1000 genomes] |
rs716103 | 1.00[AFR][1000 genomes] |
rs716104 | 1.00[AFR][1000 genomes] |
rs7925870 | 0.91[EUR][1000 genomes] |
rs7926784 | 0.91[EUR][1000 genomes] |
rs7929811 | 0.91[EUR][1000 genomes] |
rs7931694 | 0.91[EUR][1000 genomes] |
rs7935009 | 0.91[EUR][1000 genomes] |
rs7936720 | 0.91[CEU][hapmap] |
rs7937610 | 0.91[EUR][1000 genomes] |
rs7942859 | 0.91[EUR][1000 genomes] |
rs7942981 | 0.91[EUR][1000 genomes] |
rs7943492 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7945499 | 0.91[EUR][1000 genomes] |
rs7948567 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7949262 | 0.91[EUR][1000 genomes] |
rs9665861 | 0.90[CEU][hapmap] |
rs9666086 | 0.90[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1067779 | chr11:55086995-55980406 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 66 gene(s) | inside rSNPs | diseases |
2 | nsv491694 | chr11:55086995-55980406 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 66 gene(s) | inside rSNPs | diseases |
3 | nsv1036666 | chr11:55460788-56010187 | ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
4 | nsv1049004 | chr11:55460788-56014767 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 45 gene(s) | inside rSNPs | diseases |
5 | esv2830217 | chr11:55460788-56017908 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 45 gene(s) | inside rSNPs | diseases |
6 | nsv1043441 | chr11:55468512-56010187 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
7 | esv2752628 | chr11:55682604-55948184 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
8 | nsv975114 | chr11:55751535-56124251 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 32 gene(s) | inside rSNPs | diseases |
9 | nsv521440 | chr11:55763943-56052521 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
10 | nsv832160 | chr11:55780185-55916798 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 13 gene(s) | inside rSNPs | diseases |
11 | nsv949437 | chr11:55780469-56042980 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
12 | nsv1036290 | chr11:55807948-55934985 | Weak transcription Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 13 gene(s) | inside rSNPs | diseases |
13 | esv2754280 | chr11:55823576-55927591 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 10 gene(s) | inside rSNPs | diseases |
14 | esv2752700 | chr11:55830265-55896015 | Enhancers Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 7 gene(s) | inside rSNPs | diseases |
15 | nsv468575 | chr11:55847945-55937954 | Active TSS Enhancers | TF binding regionCpG islandChromatin interactive region | 11 gene(s) | inside rSNPs | diseases |
16 | nsv555095 | chr11:55847945-55937954 | Enhancers Active TSS | TF binding regionCpG islandChromatin interactive region | 11 gene(s) | inside rSNPs | diseases |
17 | esv3410489 | chr11:55872880-55890198 | Inactive region | TF binding regionCpG island | 2 gene(s) | inside rSNPs | diseases |
No data |