Variant report
Variant | rs275597 |
---|---|
Chromosome Location | chr11:45611061-45611062 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:45608873..45611223-chr11:45614271..45615865,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10742762 | 1.00[ASN][1000 genomes] |
rs10742763 | 1.00[ASN][1000 genomes] |
rs10769161 | 1.00[ASN][1000 genomes] |
rs10769162 | 1.00[ASN][1000 genomes] |
rs10838493 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10838494 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10838495 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10838496 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10838497 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038524 | 1.00[ASN][1000 genomes] |
rs11038525 | 1.00[ASN][1000 genomes] |
rs11038528 | 1.00[ASN][1000 genomes] |
rs11038530 | 1.00[ASN][1000 genomes] |
rs11038531 | 1.00[ASN][1000 genomes] |
rs11038533 | 1.00[ASN][1000 genomes] |
rs11038538 | 1.00[ASN][1000 genomes] |
rs11038539 | 1.00[ASN][1000 genomes] |
rs11038543 | 1.00[ASN][1000 genomes] |
rs11038544 | 1.00[ASN][1000 genomes] |
rs11038549 | 1.00[ASN][1000 genomes] |
rs11038550 | 1.00[ASN][1000 genomes] |
rs11038552 | 1.00[ASN][1000 genomes] |
rs11038559 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038560 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038563 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038566 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038567 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038568 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038569 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038570 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038571 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038572 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038573 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038575 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038576 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038581 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038582 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038594 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038596 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038598 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038599 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038600 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038601 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038603 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11038606 | 1.00[ASN][1000 genomes] |
rs11038615 | 1.00[ASN][1000 genomes] |
rs12362568 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12362984 | 1.00[ASN][1000 genomes] |
rs12363116 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12363231 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12364128 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12364847 | 1.00[ASN][1000 genomes] |
rs12365421 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12365436 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12365703 | 1.00[ASN][1000 genomes] |
rs12366014 | 1.00[ASN][1000 genomes] |
rs1387058 | 1.00[ASN][1000 genomes] |
rs1488677 | 1.00[ASN][1000 genomes] |
rs1562461 | 1.00[ASN][1000 genomes] |
rs17724240 | 1.00[ASN][1000 genomes] |
rs17724446 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17786178 | 1.00[ASN][1000 genomes] |
rs17786436 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2028985 | 1.00[ASN][1000 genomes] |
rs45627537 | 1.00[ASN][1000 genomes] |
rs4756007 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4756013 | 1.00[ASN][1000 genomes] |
rs4756014 | 1.00[ASN][1000 genomes] |
rs6485637 | 1.00[ASN][1000 genomes] |
rs7104214 | 1.00[ASN][1000 genomes] |
rs7105647 | 1.00[ASN][1000 genomes] |
rs7116428 | 1.00[ASN][1000 genomes] |
rs7121818 | 1.00[ASN][1000 genomes] |
rs7121848 | 1.00[ASN][1000 genomes] |
rs72895235 | 1.00[ASN][1000 genomes] |
rs72895236 | 1.00[ASN][1000 genomes] |
rs72895273 | 1.00[ASN][1000 genomes] |
rs72896754 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72896772 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72896789 | 1.00[ASN][1000 genomes] |
rs72898653 | 1.00[ASN][1000 genomes] |
rs72898676 | 1.00[ASN][1000 genomes] |
rs72899255 | 1.00[ASN][1000 genomes] |
rs72899271 | 1.00[ASN][1000 genomes] |
rs72899280 | 1.00[ASN][1000 genomes] |
rs72904957 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72904980 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72904984 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72904993 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72904994 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72904997 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72910675 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72910679 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7947626 | 1.00[ASN][1000 genomes] |
rs895718 | 1.00[ASN][1000 genomes] |
rs901907 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv897310 | chr11:45487041-45631953 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:45608200-45611800 | Weak transcription | Fetal Brain Male | brain |
2 | chr11:45609000-45611200 | Weak transcription | Brain Germinal Matrix | brain |
3 | chr11:45609400-45614000 | Weak transcription | Fetal Brain Female | brain |