Variant report
Variant | rs10501336 |
---|---|
Chromosome Location | chr11:55315519-55315520 |
allele | 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] |
---|---|
rs11823401 | 1.00[EUR][1000 genomes] |
rs11827117 | 1.00[EUR][1000 genomes] |
rs11828727 | 0.97[EUR][1000 genomes] |
rs1425195 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs1459106 | 1.00[CEU][hapmap] |
rs17494536 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17494990 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17496160 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17496724 | 1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs17498098 | 1.00[AFR][1000 genomes] |
rs17498161 | 1.00[AFR][1000 genomes] |
rs17498926 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs17579334 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17579348 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17579755 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17579825 | 1.00[EUR][1000 genomes] |
rs17580966 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17580994 | 1.00[EUR][1000 genomes] |
rs17581051 | 1.00[EUR][1000 genomes] |
rs17581261 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17581303 | 1.00[CEU][hapmap] |
rs17581532 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs17581700 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs17582140 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2169004 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs488213 | 0.97[EUR][1000 genomes] |
rs492647 | 0.93[EUR][1000 genomes] |
rs505338 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs530679 | 0.97[EUR][1000 genomes] |
rs548768 | 0.97[EUR][1000 genomes] |
rs55770365 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55946210 | 1.00[AFR][1000 genomes] |
rs55972122 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56045005 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56063922 | 1.00[EUR][1000 genomes] |
rs56333107 | 1.00[EUR][1000 genomes] |
rs61895192 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61895193 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61895194 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs61895225 | 0.85[AMR][1000 genomes] |
rs61896972 | 1.00[AFR][1000 genomes] |
rs61896978 | 1.00[AFR][1000 genomes] |
rs61916282 | 1.00[EUR][1000 genomes] |
rs61916283 | 1.00[EUR][1000 genomes] |
rs61916284 | 1.00[EUR][1000 genomes] |
rs61916285 | 0.97[EUR][1000 genomes] |
rs61916286 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61916289 | 1.00[EUR][1000 genomes] |
rs61916290 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61916319 | 1.00[EUR][1000 genomes] |
rs61916320 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61916321 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61916328 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61916398 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916400 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916402 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916403 | 0.80[EUR][1000 genomes] |
rs61916404 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916405 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916412 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916413 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs61916455 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61916565 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61917939 | 1.00[EUR][1000 genomes] |
rs61917940 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61917941 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61917942 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61917986 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61917987 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61917988 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61917989 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61917998 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs61918237 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs61919565 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7103342 | 0.95[EUR][1000 genomes] |
rs7106100 | 0.80[EUR][1000 genomes] |
rs7109287 | 0.80[EUR][1000 genomes] |
rs7110861 | 1.00[EUR][1000 genomes] |
rs7111663 | 0.80[EUR][1000 genomes] |
rs7111681 | 0.80[EUR][1000 genomes] |
rs7115527 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7119347 | 1.00[EUR][1000 genomes] |
rs7121555 | 1.00[EUR][1000 genomes] |
rs7127405 | 1.00[CEU][hapmap];1.00[TSI][hapmap] |
rs7924882 | 0.80[EUR][1000 genomes] |
rs7929411 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs7929606 | 1.00[EUR][1000 genomes] |
rs7930341 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7940290 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7940305 | 1.00[EUR][1000 genomes] |
rs7940435 | 1.00[EUR][1000 genomes] |
rs7940928 | 0.80[EUR][1000 genomes] |
rs7941275 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7941839 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7941860 | 1.00[EUR][1000 genomes] |
rs7943092 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7946976 | 1.00[CEU][hapmap] |
rs7948802 | 0.80[EUR][1000 genomes] |
rs7949637 | 1.00[AFR][1000 genomes] |
rs7949664 | 1.00[AFR][1000 genomes] |
rs7950685 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7950755 | 1.00[EUR][1000 genomes] |
rs7950956 | 0.97[EUR][1000 genomes] |
rs9666121 | 1.00[EUR][1000 genomes] |
rs9666260 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9666744 | 1.00[EUR][1000 genomes] |
rs9667732 | 1.00[EUR][1000 genomes] |
rs982276 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2830215 | chr11:54711990-55340379 | ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
2 | nsv1052144 | chr11:54720811-55438474 | ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
3 | nsv1053949 | chr11:54773881-55363328 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
4 | nsv1051643 | chr11:54826801-55363328 | ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
5 | nsv524091 | chr11:54875038-55522549 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | diseases |
6 | 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 |
7 | nsv975110 | chr11:55076487-55318108 | ZNF genes & repeats Active TSS Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive region | 17 gene(s) | inside rSNPs | diseases |
8 | nsv467886 | chr11:55083434-55408700 | Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 19 gene(s) | inside rSNPs | diseases |
9 | nsv554799 | chr11:55083434-55408700 | Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription | TF binding regionCpG islandChromatin interactive region | 19 gene(s) | inside rSNPs | diseases |
10 | nsv554800 | chr11:55083434-55695985 | ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 42 gene(s) | inside rSNPs | diseases |
11 | nsv916012 | chr11:55084067-55622531 | ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer Enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 36 gene(s) | inside rSNPs | diseases |
12 | 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 |
13 | 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 |
14 | nsv1036325 | chr11:55119267-55442306 | ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer | TF binding regionCpG island | 19 gene(s) | inside rSNPs | diseases |
15 | esv2751031 | chr11:55121706-55340753 | Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription | TF binding regionCpG island | 14 gene(s) | inside rSNPs | diseases |
16 | nsv821668 | chr11:55153930-55816828 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 46 gene(s) | inside rSNPs | diseases |
17 | nsv518225 | chr11:55171677-55408700 | ZNF genes & repeats Active TSS Bivalent Enhancer Weak transcription Enhancers | TF binding regionCpG island | 14 gene(s) | inside rSNPs | diseases |
18 | esv2758271 | chr11:55222420-55621884 | Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
19 | esv2759828 | chr11:55222420-55638112 | ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
20 | nsv832154 | chr11:55222427-55408933 | Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription | TF binding regionCpG island | 10 gene(s) | inside rSNPs | diseases |
21 | nsv1046475 | chr11:55241003-55381810 | ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Enhancers | TF binding regionCpG island | 8 gene(s) | inside rSNPs | diseases |
22 | nsv1047882 | chr11:55241003-55386385 | Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer | TF binding regionCpG island | 8 gene(s) | inside rSNPs | diseases |
23 | esv2751032 | chr11:55276602-55355722 | ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer | TF binding regionCpG island | 4 gene(s) | inside rSNPs | diseases |
24 | nsv832155 | chr11:55277241-55432666 | Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer | TF binding regionCpG island | 7 gene(s) | inside rSNPs | diseases |
25 | nsv916314 | chr11:55289861-55495986 | ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
26 | nsv1048237 | chr11:55312533-55363328 | ZNF genes & repeats Bivalent Enhancer Enhancers | TF binding regionCpG island | 2 gene(s) | inside rSNPs | diseases |
27 | nsv554801 | chr11:55314151-55624360 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:55312200-55315800 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |