| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv869023 |
chr4:91940838-92935383 |
Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
14 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3384271 |
chr4:92073391-92464275 |
Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv879566 |
chr4:92215966-92322333 |
ZNF genes & repeats Enhancers Weak transcription
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv879567 |
chr4:92215966-92413671 |
ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv522208 |
chr4:92241587-92283771 |
ZNF genes & repeats Enhancers Weak transcription
|
TF binding regionChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
esv1830673 |
chr4:92241587-92379081 |
Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv879568 |
chr4:92244300-92429961 |
Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
nsv529020 |
chr4:92253926-92293482 |
Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv594849 |
chr4:92271993-92285150 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv966558 |
chr4:92273882-92285480 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv515874 |
chr4:92280933-92283771 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv818252 |
chr4:92280933-92283771 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv594850 |
chr4:92280933-92284120 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv594851 |
chr4:92280933-92284935 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv594852 |
chr4:92280933-92285077 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv594853 |
chr4:92280933-92285150 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv594854 |
chr4:92280933-92286445 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv594855 |
chr4:92280933-92286553 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv461584 |
chr4:92280933-92344220 |
ZNF genes & repeats Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv594856 |
chr4:92280933-92344220 |
Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page:
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