| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv1793412 |
chr8:66705321-66761366 |
Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
22 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3446467 |
chr8:66749863-67667068 |
Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
73 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
esv3479393 |
chr8:66759049-66760714 |
Weak transcription Enhancers
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
esv3479395 |
chr8:66759351-66760468 |
Weak transcription Enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv3479394 |
chr8:66759425-66760415 |
Weak transcription Enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
esv3479398 |
chr8:66759478-66760352 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
esv16780 |
chr8:66759486-66760364 |
Enhancers Weak transcription
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
esv3479399 |
chr8:66759492-66760351 |
Weak transcription Enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 9 |
nsv611455 |
chr8:66759523-66760147 |
Weak transcription Enhancers
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 10 |
nsv611456 |
chr8:66759626-66772558 |
Weak transcription Enhancers Flanking Active TSS
|
Chromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page:
1
