No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
esv3316809 |
chr18:45099773-45100312 |
Bivalent Enhancer Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
2 |
esv3493646 |
chr18:45099820-45100256 |
Weak transcription Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
3 |
esv3493647 |
chr18:45099820-45100256 |
Weak transcription Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
4 |
esv3316806 |
chr18:45099829-45100274 |
Bivalent Enhancer Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
5 |
esv3316808 |
chr18:45099829-45100278 |
Weak transcription Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
6 |
esv3316810 |
chr18:45099842-45100230 |
Weak transcription Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
7 |
esv3347040 |
chr18:45099861-45100231 |
Bivalent Enhancer Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
8 |
esv3316811 |
chr18:45099881-45100211 |
Weak transcription Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
9 |
esv3316812 |
chr18:45099895-45100221 |
Weak transcription Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
10 |
nsv120822 |
chr18:45100189-45100190 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|