| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv890955 |
chr8:62919691-63062581 |
Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
esv3490106 |
chr8:63033798-63041596 |
Enhancers Bivalent Enhancer Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv3490111 |
chr8:63034248-63041446 |
Weak transcription Enhancers Bivalent Enhancer
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3490107 |
chr8:63034802-63040502 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3479350 |
chr8:63034841-63040500 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3490109 |
chr8:63034866-63040463 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3479353 |
chr8:63034870-63040468 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv3479349 |
chr8:63034886-63040439 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3490112 |
chr8:63034896-63040463 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3490110 |
chr8:63034896-63040464 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3479351 |
chr8:63034933-63040397 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3479354 |
chr8:63034947-63040399 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv611428 |
chr8:63034992-63038096 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv611429 |
chr8:63034992-63038398 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv611430 |
chr8:63034992-63038700 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv611431 |
chr8:63034992-63039018 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv611432 |
chr8:63034992-63039350 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv611433 |
chr8:63034992-63039587 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv611434 |
chr8:63034992-63039751 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv611435 |
chr8:63034992-63039968 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv611436 |
chr8:63034992-63040410 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv12888 |
chr8:63034999-63040375 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
nsv968535 |
chr8:63035169-63039062 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
nsv611437 |
chr8:63035265-63039350 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
nsv611438 |
chr8:63035265-63039587 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
nsv611439 |
chr8:63035265-63039751 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
nsv611440 |
chr8:63035856-63039751 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
nsv611441 |
chr8:63035856-63039968 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
nsv611442 |
chr8:63036140-63039968 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 30 |
nsv611443 |
chr8:63036600-63039751 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 31 |
nsv611444 |
chr8:63036886-63039968 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page:
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