Variant report
Variant | rs61891195 |
---|---|
Chromosome Location | chr11:55826530-55826531 |
allele | A/C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12099295 | 0.91[EUR][1000 genomes] |
rs17514608 | 0.91[EUR][1000 genomes] |
rs17527401 | 0.91[EUR][1000 genomes] |
rs17527710 | 0.89[EUR][1000 genomes] |
rs17527788 | 0.91[EUR][1000 genomes] |
rs17527850 | 0.91[EUR][1000 genomes] |
rs17527864 | 0.91[EUR][1000 genomes] |
rs17528782 | 0.94[EUR][1000 genomes] |
rs17528803 | 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 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17530423 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17596694 | 0.89[EUR][1000 genomes] |
rs17597646 | 0.89[EUR][1000 genomes] |
rs17598017 | 0.89[EUR][1000 genomes] |
rs17598045 | 0.89[EUR][1000 genomes] |
rs17598094 | 0.89[EUR][1000 genomes] |
rs17599457 | 0.91[EUR][1000 genomes] |
rs17599471 | 0.91[EUR][1000 genomes] |
rs17599899 | 0.91[EUR][1000 genomes] |
rs17599913 | 0.91[EUR][1000 genomes] |
rs17600692 | 0.94[EUR][1000 genomes] |
rs17600784 | 0.94[EUR][1000 genomes] |
rs17600820 | 0.94[EUR][1000 genomes] |
rs17603011 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1947923 | 0.94[EUR][1000 genomes] |
rs2449138 | 0.94[EUR][1000 genomes] |
rs2512932 | 0.94[EUR][1000 genomes] |
rs28421520 | 1.00[EUR][1000 genomes] |
rs28537497 | 1.00[EUR][1000 genomes] |
rs28688517 | 1.00[EUR][1000 genomes] |
rs5018553 | 0.91[EUR][1000 genomes] |
rs55696205 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55833459 | 0.91[EUR][1000 genomes] |
rs55833816 | 0.89[EUR][1000 genomes] |
rs56057397 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][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] |
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] |
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] |
rs61894170 | 0.89[EUR][1000 genomes] |
rs61894171 | 0.89[EUR][1000 genomes] |
rs61894172 | 0.89[EUR][1000 genomes] |
rs61894173 | 0.89[EUR][1000 genomes] |
rs61894174 | 0.89[EUR][1000 genomes] |
rs61894176 | 0.89[EUR][1000 genomes] |
rs61894198 | 0.89[EUR][1000 genomes] |
rs61894199 | 0.89[EUR][1000 genomes] |
rs61894201 | 0.89[EUR][1000 genomes] |
rs61894202 | 0.89[EUR][1000 genomes] |
rs61894203 | 0.89[EUR][1000 genomes] |
rs61894213 | 0.89[EUR][1000 genomes] |
rs61894214 | 0.89[EUR][1000 genomes] |
rs61894215 | 0.89[EUR][1000 genomes] |
rs61894216 | 0.87[EUR][1000 genomes] |
rs61895181 | 0.91[EUR][1000 genomes] |
rs61895182 | 0.91[EUR][1000 genomes] |
rs61895183 | 0.91[EUR][1000 genomes] |
rs61895184 | 0.91[EUR][1000 genomes] |
rs61895240 | 0.91[EUR][1000 genomes] |
rs61895241 | 0.91[EUR][1000 genomes] |
rs61895243 | 0.91[EUR][1000 genomes] |
rs61895244 | 0.91[EUR][1000 genomes] |
rs61895245 | 0.91[EUR][1000 genomes] |
rs61895246 | 0.91[EUR][1000 genomes] |
rs61895247 | 0.91[EUR][1000 genomes] |
rs61895248 | 0.91[EUR][1000 genomes] |
rs61895249 | 0.91[EUR][1000 genomes] |
rs61895250 | 0.87[EUR][1000 genomes] |
rs61895251 | 0.91[EUR][1000 genomes] |
rs61895252 | 0.91[EUR][1000 genomes] |
rs61895253 | 0.91[EUR][1000 genomes] |
rs61895254 | 0.91[EUR][1000 genomes] |
rs61895255 | 0.91[EUR][1000 genomes] |
rs61895256 | 0.91[EUR][1000 genomes] |
rs61895257 | 0.91[EUR][1000 genomes] |
rs61895258 | 0.91[EUR][1000 genomes] |
rs61895259 | 0.91[EUR][1000 genomes] |
rs61896168 | 0.91[EUR][1000 genomes] |
rs61896169 | 0.91[EUR][1000 genomes] |
rs61896182 | 0.91[EUR][1000 genomes] |
rs61896183 | 0.91[EUR][1000 genomes] |
rs61896184 | 0.91[EUR][1000 genomes] |
rs61896235 | 0.91[EUR][1000 genomes] |
rs61896236 | 0.89[EUR][1000 genomes] |
rs61896237 | 0.91[EUR][1000 genomes] |
rs61896238 | 0.91[EUR][1000 genomes] |
rs61896240 | 0.91[EUR][1000 genomes] |
rs61896241 | 0.91[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] |
rs7109807 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
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] |
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] |
rs7128453 | 0.94[EUR][1000 genomes] |
rs7131505 | 0.92[EUR][1000 genomes] |
rs7131616 | 0.92[EUR][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] |
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] |
rs9666864 | 0.89[EUR][1000 genomes] |
rs9667335 | 0.89[EUR][1000 genomes] |
rs9667688 | 0.89[EUR][1000 genomes] |
rs9667699 | 0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv554797 | chr11:55035411-55864161 | Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 59 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | nsv1044174 | chr11:55501796-55862172 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
9 | nsv437718 | chr11:55679983-55828756 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
10 | 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 |
11 | nsv517590 | chr11:55685556-55836620 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
12 | nsv1053326 | chr11:55685799-55829456 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
13 | esv34592 | chr11:55685799-55842512 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
14 | esv34825 | chr11:55685824-55842512 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
15 | nsv1047031 | chr11:55689110-55827538 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
16 | esv2757446 | chr11:55689863-55849156 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
17 | esv2759829 | chr11:55689863-55849156 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
18 | 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 |
19 | 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 |
20 | nsv832160 | chr11:55780185-55916798 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 13 gene(s) | inside rSNPs | diseases |
21 | 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 |
22 | nsv1036290 | chr11:55807948-55934985 | Weak transcription Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 13 gene(s) | inside rSNPs | diseases |
23 | esv2754280 | chr11:55823576-55927591 | Flanking Active TSS Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:55822800-55834000 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
2 | chr11:55824800-55827200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
3 | chr11:55825200-55828600 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
4 | chr11:55825800-55826800 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
5 | chr11:55825800-55827200 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
6 | chr11:55826000-55827600 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
7 | chr11:55826400-55827600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |