Variant report
Variant | rs10172981 |
---|---|
Chromosome Location | chr2:77223148-77223149 |
allele | A/G |
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] |
---|---|
rs10208087 | 0.92[EUR][1000 genomes] |
rs10520177 | 0.92[EUR][1000 genomes] |
rs1075716 | 0.91[EUR][1000 genomes] |
rs1077111 | 0.92[EUR][1000 genomes] |
rs13388459 | 1.00[YRI][hapmap];0.95[EUR][1000 genomes] |
rs13413951 | 1.00[YRI][hapmap];0.95[EUR][1000 genomes] |
rs1345137 | 0.86[EUR][1000 genomes] |
rs1446708 | 0.88[EUR][1000 genomes] |
rs1446721 | 0.92[EUR][1000 genomes] |
rs17013567 | 0.87[EUR][1000 genomes] |
rs17013635 | 0.83[EUR][1000 genomes] |
rs17333926 | 0.87[EUR][1000 genomes] |
rs17334205 | 0.92[EUR][1000 genomes] |
rs17334240 | 0.92[EUR][1000 genomes] |
rs17334254 | 0.92[EUR][1000 genomes] |
rs17334261 | 0.92[EUR][1000 genomes] |
rs17334527 | 0.85[EUR][1000 genomes] |
rs17405864 | 0.90[EUR][1000 genomes] |
rs17405905 | 0.92[EUR][1000 genomes] |
rs17405953 | 0.92[EUR][1000 genomes] |
rs17405981 | 0.92[EUR][1000 genomes] |
rs17406023 | 0.92[EUR][1000 genomes] |
rs17406084 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17406091 | 0.91[EUR][1000 genomes] |
rs17406146 | 0.91[EUR][1000 genomes] |
rs17406202 | 0.90[EUR][1000 genomes] |
rs17406374 | 0.87[EUR][1000 genomes] |
rs1929456 | 0.82[CEU][hapmap] |
rs1929458 | 0.81[CEU][hapmap] |
rs1960005 | 0.87[EUR][1000 genomes] |
rs2077823 | 0.87[EUR][1000 genomes] |
rs34007251 | 1.00[CEU][hapmap];0.93[EUR][1000 genomes] |
rs4396752 | 0.92[EUR][1000 genomes] |
rs4401235 | 0.92[EUR][1000 genomes] |
rs4447628 | 0.92[EUR][1000 genomes] |
rs4491748 | 0.91[EUR][1000 genomes] |
rs4637153 | 0.81[CEU][hapmap];0.92[EUR][1000 genomes] |
rs55800138 | 0.87[EUR][1000 genomes] |
rs55864802 | 0.83[EUR][1000 genomes] |
rs62170208 | 0.90[EUR][1000 genomes] |
rs62170209 | 0.89[EUR][1000 genomes] |
rs62170210 | 0.90[EUR][1000 genomes] |
rs62170864 | 0.90[EUR][1000 genomes] |
rs62170865 | 0.90[EUR][1000 genomes] |
rs62170866 | 0.90[EUR][1000 genomes] |
rs62170872 | 0.86[EUR][1000 genomes] |
rs62170895 | 0.87[EUR][1000 genomes] |
rs62170896 | 0.87[EUR][1000 genomes] |
rs62170899 | 0.86[EUR][1000 genomes] |
rs62171961 | 0.92[EUR][1000 genomes] |
rs62171964 | 0.92[EUR][1000 genomes] |
rs62171994 | 0.90[EUR][1000 genomes] |
rs62171995 | 0.92[EUR][1000 genomes] |
rs62171996 | 0.92[EUR][1000 genomes] |
rs62171997 | 0.92[EUR][1000 genomes] |
rs66769122 | 0.91[EUR][1000 genomes] |
rs6742824 | 0.92[EUR][1000 genomes] |
rs72823135 | 0.88[EUR][1000 genomes] |
rs72823137 | 0.88[EUR][1000 genomes] |
rs72823174 | 0.92[EUR][1000 genomes] |
rs72823176 | 0.88[EUR][1000 genomes] |
rs72823182 | 0.91[EUR][1000 genomes] |
rs72823183 | 0.91[EUR][1000 genomes] |
rs72823195 | 0.87[EUR][1000 genomes] |
rs72823196 | 0.87[EUR][1000 genomes] |
rs72823197 | 0.87[EUR][1000 genomes] |
rs953855 | 0.82[CEU][hapmap] |
rs956657 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834266 | chr2:77120236-77287504 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv949670 | chr2:77125218-77712607 | Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv519950 | chr2:77213103-77256291 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv829468 | chr2:77216448-77224533 | Weak transcription Enhancers | lncRNA | n/a | inside rSNPs | diseases |
5 | nsv961764 | chr2:77216571-77228053 | Enhancers Weak transcription | lncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:77222800-77224400 | Enhancers | Pancreatic Islets | Pancreatic Islet |