| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv583952 |
chr2:184495927-184594404 |
Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
nsv869960 |
chr2:184502527-184639318 |
Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv527180 |
chr2:184556456-184581876 |
Weak transcription Enhancers Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
| 4 |
nsv1013775 |
chr2:184571298-184613057 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 5 |
nsv1006014 |
chr2:184571298-184614354 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 6 |
nsv583953 |
chr2:184573149-184608315 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
n/a
|
| 7 |
nsv1007281 |
chr2:184573763-184638716 |
Enhancers Flanking Bivalent TSS/Enh
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
