| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv530038 |
chr14:37590543-38336191 |
Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
58 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv916985 |
chr14:38052347-38838551 |
Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
59 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv564385 |
chr14:38246440-38321607 |
Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv1040555 |
chr14:38271184-38314601 |
Enhancers Weak transcription Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv901650 |
chr14:38289942-38331900 |
Enhancers Weak transcription
|
TF binding regionChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
