| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1013365 |
chr4:20834054-21609078 |
Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv829879 |
chr4:21418568-21611002 |
Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv998481 |
chr4:21421945-21608805 |
Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv829880 |
chr4:21492426-21693816 |
Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv878750 |
chr4:21492445-21520250 |
Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 6 |
nsv963593 |
chr4:21509366-21510666 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
