| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv875783 |
chr2:212530466-212564895 |
Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS
|
TF binding region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3417917 |
chr2:212550607-212552555 |
ZNF genes & repeats Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv2519305 |
chr2:212550857-212552523 |
Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv7939 |
chr2:212550983-212551706 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv2098674 |
chr2:212551067-212551750 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3403918 |
chr2:212551107-212552055 |
Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3459084 |
chr2:212551130-212551626 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3501738 |
chr2:212551146-212551628 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3425040 |
chr2:212551149-212551657 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3501742 |
chr2:212551172-212551598 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3501737 |
chr2:212551174-212551579 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3459081 |
chr2:212551189-212551614 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3501739 |
chr2:212551194-212551599 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3459082 |
chr2:212551196-212551570 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3501743 |
chr2:212551201-212551600 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3366017 |
chr2:212551209-212551564 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3459083 |
chr2:212551229-212551552 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv4037 |
chr2:212551230-212551601 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3501740 |
chr2:212551245-212551543 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv2567329 |
chr2:212551246-212551542 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv213952 |
chr2:212551246-212551542 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3459085 |
chr2:212551246-212551558 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3501744 |
chr2:212551246-212551558 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv1034805 |
chr2:212551260-212551557 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page:
1
