| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv899499 |
chr12:105616297-105722529 |
Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
17 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1044450 |
chr12:105668451-105682822 |
Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv510589 |
chr12:105670071-105743755 |
Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv3492286 |
chr12:105680848-105681708 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3511409 |
chr12:105680886-105681685 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3511412 |
chr12:105680897-105681633 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3492274 |
chr12:105680905-105681674 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3656 |
chr12:105680909-105681748 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3492241 |
chr12:105680914-105681669 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3492252 |
chr12:105680917-105681633 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3511410 |
chr12:105680922-105681649 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3511411 |
chr12:105680926-105681647 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv826508 |
chr12:105680952-105681730 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3492263 |
chr12:105680967-105681604 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3511413 |
chr12:105680977-105681605 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3492297 |
chr12:105680981-105681603 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3511414 |
chr12:105680981-105681603 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3381379 |
chr12:105680987-105681708 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv16955 |
chr12:105680990-105681599 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page:
1
