Variant report
Variant | rs72909215 |
---|---|
Chromosome Location | chr3:85532533-85532534 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:85528291..85540418-chr3:85548148..85554862,16 | K562 | blood: | |
2 | chr3:85531519..85533472-chr3:85537388..85539522,2 | K562 | blood: | |
3 | chr3:85525792..85532904-chr3:85548163..85554926,11 | K562 | blood: | |
4 | chr3:85527157..85529788-chr3:85532322..85535724,4 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10511080 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11918831 | 1.00[AMR][1000 genomes] |
rs11922348 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11929389 | 1.00[AMR][1000 genomes] |
rs1449392 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17022855 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17022902 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17022958 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17023026 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28568871 | 1.00[AMR][1000 genomes] |
rs56825201 | 1.00[AMR][1000 genomes] |
rs57611991 | 1.00[AMR][1000 genomes] |
rs58154502 | 1.00[AMR][1000 genomes] |
rs58690958 | 1.00[AMR][1000 genomes] |
rs59142599 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59326245 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60012465 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60048765 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60195286 | 1.00[AMR][1000 genomes] |
rs60365981 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61153638 | 1.00[EUR][1000 genomes] |
rs6781652 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6795136 | 1.00[EUR][1000 genomes] |
rs72903276 | 1.00[AMR][1000 genomes] |
rs72903287 | 1.00[AMR][1000 genomes] |
rs72905414 | 1.00[AMR][1000 genomes] |
rs72905427 | 1.00[AMR][1000 genomes] |
rs72905447 | 1.00[AMR][1000 genomes] |
rs72905453 | 1.00[AMR][1000 genomes] |
rs72905457 | 1.00[AMR][1000 genomes] |
rs72905465 | 1.00[AMR][1000 genomes] |
rs72905473 | 1.00[AMR][1000 genomes] |
rs72905474 | 1.00[AMR][1000 genomes] |
rs72905475 | 1.00[AMR][1000 genomes] |
rs72909239 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909241 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909262 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909263 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909291 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909292 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909296 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909298 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72909301 | 1.00[AMR][1000 genomes] |
rs72911210 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72911212 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs72911213 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72913150 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72913155 | 1.00[EUR][1000 genomes] |
rs72913158 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72913172 | 1.00[EUR][1000 genomes] |
rs73843636 | 1.00[EUR][1000 genomes] |
rs73843645 | 1.00[EUR][1000 genomes] |
rs7613186 | 1.00[AMR][1000 genomes] |
rs7626074 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7636650 | 0.87[AFR][1000 genomes];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 | esv3419993 | chr3:85030343-85663403 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv2753915 | chr3:85071410-85624810 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1002238 | chr3:85357855-85719373 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv536619 | chr3:85357855-85719373 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv590904 | chr3:85438564-85551403 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv590905 | chr3:85438564-85797093 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv998829 | chr3:85449960-85641099 | Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv536622 | chr3:85449960-85641099 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv526621 | chr3:85470642-85667683 | Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | nsv1009512 | chr3:85472690-85533487 | Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
11 | nsv536623 | chr3:85472690-85533487 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
12 | nsv1013601 | chr3:85489536-85570465 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
13 | nsv536624 | chr3:85489536-85570465 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
14 | nsv1009927 | chr3:85497666-85669155 | Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | nsv1010541 | chr3:85505839-85870597 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
16 | nsv536625 | chr3:85505839-85870597 | Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
17 | esv2762338 | chr3:85520915-85577233 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
18 | nsv1009804 | chr3:85521984-85581386 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
19 | nsv536626 | chr3:85527837-85578368 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:85519200-85536800 | Weak transcription | Fetal Brain Male | brain |
2 | chr3:85531000-85534600 | Weak transcription | HSMM | muscle |
3 | chr3:85531200-85533000 | Weak transcription | Osteobl | bone |
4 | chr3:85531400-85533000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr3:85531600-85533600 | Weak transcription | K562 | blood |
6 | chr3:85531800-85533200 | Weak transcription | Muscle Satellite Cultured Cells | -- |
7 | chr3:85531800-85533400 | Weak transcription | Brain Angular Gyrus | brain |