| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv468149 |
chr1:217134966-217203091 |
Enhancers Weak transcription
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
nsv549204 |
chr1:217134966-217203091 |
Weak transcription Enhancers
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv428610 |
chr1:217143317-217307243 |
Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv1008670 |
chr1:217155114-217206765 |
Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
nsv1012243 |
chr1:217157000-217206765 |
Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv1006155 |
chr1:217157000-217215465 |
Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS
|
Chromatin interactive regionlncRNA
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv159053 |
chr1:217157029-217157030 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
