| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv529328 |
chr12:29692414-30246209 |
Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
8 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv898953 |
chr12:29905322-29989292 |
Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv469191 |
chr12:29939628-30098770 |
Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv557958 |
chr12:29939628-30098770 |
ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS
|
TF binding regionCpG islandChromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv557959 |
chr12:29944670-29959697 |
Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv15301 |
chr12:29956430-29960234 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
nsv557961 |
chr12:29956687-29959419 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv1793972 |
chr12:29956687-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv1799080 |
chr12:29956687-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv1801015 |
chr12:29956687-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv1803861 |
chr12:29956687-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv557962 |
chr12:29956687-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv557963 |
chr12:29956687-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv557964 |
chr12:29956687-29971416 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv1791821 |
chr12:29957034-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv1797798 |
chr12:29957034-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv1798426 |
chr12:29957034-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv1799970 |
chr12:29957034-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv1802535 |
chr12:29957034-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv1804095 |
chr12:29957034-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv557967 |
chr12:29957068-29959419 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv1801773 |
chr12:29957068-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv1802355 |
chr12:29957068-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
nsv557968 |
chr12:29957068-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
nsv557969 |
chr12:29957068-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
nsv557970 |
chr12:29957119-29959419 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
nsv557971 |
chr12:29957172-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
nsv557973 |
chr12:29957458-29959697 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
nsv557974 |
chr12:29957710-29959567 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page:
1
