| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv2751288 |
chr14:84815330-85704047 |
Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
6 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1046875 |
chr14:84993510-85193250 |
Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats
|
Chromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv565378 |
chr14:85070611-85140984 |
Enhancers Weak transcription Active TSS Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv1829021 |
chr14:85106009-85196163 |
Enhancers Weak transcription Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3530368 |
chr14:85137199-85141497 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv2516457 |
chr14:85138146-85139948 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv1820152 |
chr14:85138430-85139498 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv1831944 |
chr14:85138430-85139498 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv1835010 |
chr14:85138430-85139498 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv1835631 |
chr14:85138430-85139498 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv1840823 |
chr14:85138430-85139498 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv1841671 |
chr14:85138430-85139498 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3516593 |
chr14:85138449-85140647 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv8527 |
chr14:85138948-85139859 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv2128931 |
chr14:85138964-85139803 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3530366 |
chr14:85139027-85139733 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3516595 |
chr14:85139027-85139736 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3516592 |
chr14:85139035-85139721 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3516597 |
chr14:85139065-85139662 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3530371 |
chr14:85139068-85139698 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3530367 |
chr14:85139075-85139695 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3516594 |
chr14:85139082-85139673 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3530365 |
chr14:85139087-85139653 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv3516598 |
chr14:85139087-85139675 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv3403301 |
chr14:85139107-85139645 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
esv3530364 |
chr14:85139131-85139631 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
esv3516591 |
chr14:85139144-85139625 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
nsv85605 |
chr14:85139146-85139625 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
esv3516599 |
chr14:85139146-85139627 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 30 |
esv3530372 |
chr14:85139146-85139627 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 31 |
nsv821291 |
chr14:85139149-85139743 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 32 |
nsv827015 |
chr14:85139149-85139743 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 33 |
esv11839 |
chr14:85139162-85139627 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 34 |
nsv819254 |
chr14:85139179-85139601 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page:
1
