| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv3388948 |
chr2:50092667-50602681 |
Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3399511 |
chr2:50092687-50602651 |
Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription
|
TF binding regionCpG islandChromatin interactive regionmiRNA target site
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv3457690 |
chr2:50134540-50135650 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3457689 |
chr2:50134586-50135627 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3457688 |
chr2:50134605-50135602 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3457691 |
chr2:50134683-50135539 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3457692 |
chr2:50134697-50135537 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv18429 |
chr2:50134719-50135515 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
