| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv606199 |
chr7:11506143-12486659 |
Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
20 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv887614 |
chr7:11778424-12211198 |
Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription
|
TF binding regionCpG islandChromatin interactive region
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv887619 |
chr7:11893588-12043231 |
Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv2758103 |
chr7:11927239-12109419 |
Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv2759510 |
chr7:11927239-12109419 |
ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
nsv887625 |
chr7:11981995-12046503 |
Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv830906 |
chr7:12001764-12177869 |
Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv2554206 |
chr7:12023291-12024808 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3448493 |
chr7:12023477-12025475 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv606222 |
chr7:12023864-12084381 |
Enhancers Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv2329154 |
chr7:12024043-12024692 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3475636 |
chr7:12024108-12024598 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv5659 |
chr7:12024134-12024604 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3491416 |
chr7:12024140-12024610 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3491414 |
chr7:12024143-12024541 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3491413 |
chr7:12024146-12024593 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3491412 |
chr7:12024158-12024536 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3475638 |
chr7:12024164-12024564 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv2895 |
chr7:12024166-12024582 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3475637 |
chr7:12024178-12024525 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3491417 |
chr7:12024178-12024555 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3384597 |
chr7:12024198-12024525 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3475639 |
chr7:12024204-12024500 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv3475635 |
chr7:12024217-12024504 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv3491415 |
chr7:12024229-12024499 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
esv3491418 |
chr7:12024231-12024514 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
esv1762584 |
chr7:12024244-12024513 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page:
1
