| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1006097 |
chr2:76524248-76675427 |
Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv519947 |
chr2:76537604-76588942 |
Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv874313 |
chr2:76540365-76591470 |
Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv2757809 |
chr2:76541920-76705354 |
Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
esv2759064 |
chr2:76541920-76705354 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv1008019 |
chr2:76542989-76586699 |
ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv2763343 |
chr2:76543001-76586711 |
Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv1007312 |
chr2:76544454-76582327 |
Enhancers Weak transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
nsv1014043 |
chr2:76544454-76585748 |
Enhancers Weak transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv1008178 |
chr2:76544454-76586332 |
Weak transcription Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv1003728 |
chr2:76544454-76586699 |
ZNF genes & repeats Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv582223 |
chr2:76545193-76588942 |
Weak transcription Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv1011137 |
chr2:76547751-76586699 |
Weak transcription Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv874314 |
chr2:76548341-76598587 |
Enhancers ZNF genes & repeats Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv874315 |
chr2:76548341-76605834 |
Weak transcription Enhancers ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv874316 |
chr2:76548341-76613885 |
ZNF genes & repeats Weak transcription Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv874317 |
chr2:76554077-76890567 |
Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 18 |
esv3439431 |
chr2:76556069-76558617 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3362975 |
chr2:76556344-76558292 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3404313 |
chr2:76556844-76557792 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3457929 |
chr2:76556922-76557387 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3487781 |
chr2:76556937-76557351 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv8258 |
chr2:76556941-76557395 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv3457931 |
chr2:76556944-76557370 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv3487785 |
chr2:76556964-76557322 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
esv3487783 |
chr2:76556964-76557370 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
esv3487782 |
chr2:76556969-76557332 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
esv3378 |
chr2:76556978-76557350 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
esv3457933 |
chr2:76556978-76557360 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 30 |
esv3457932 |
chr2:76556997-76557313 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 31 |
esv3487784 |
chr2:76556999-76557341 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 32 |
esv3374569 |
chr2:76557039-76557292 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 33 |
esv3457928 |
chr2:76557043-76557295 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 34 |
esv3487787 |
chr2:76557055-76557290 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 35 |
esv989387 |
chr2:76557057-76557290 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 36 |
esv1697288 |
chr2:76557057-76557291 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 37 |
esv3457934 |
chr2:76557057-76557292 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 38 |
esv3487788 |
chr2:76557057-76557292 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page:
1
