| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1064857 |
chr21:17628760-18533131 |
Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
345 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv544382 |
chr21:17628760-18533131 |
Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
345 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv913416 |
chr21:17728224-17863882 |
Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer
|
TF binding regionChromatin interactive regionlncRNA
|
16 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv913417 |
chr21:17762340-17777827 |
ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription
|
lncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv913418 |
chr21:17767773-17786219 |
Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3455310 |
chr21:17770886-17775518 |
Enhancers Weak transcription Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3455312 |
chr21:17770886-17775518 |
Weak transcription Enhancers Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3455311 |
chr21:17770913-17775515 |
Enhancers Weak transcription Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv828825 |
chr21:17771002-17772550 |
Weak transcription Strong transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
