No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv949248 |
chr11:17791822-18692687 |
Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site
|
156 gene(s)
|
inside rSNPs
|
diseases
|
2 |
nsv553591 |
chr11:18090519-18100022 |
Weak transcription Enhancers Strong transcription Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
3 |
nsv553593 |
chr11:18095815-18100022 |
Weak transcription Enhancers Strong transcription Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
4 |
nsv553594 |
chr11:18095815-18100799 |
Weak transcription Strong transcription Enhancers Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
5 |
nsv553596 |
chr11:18097481-18099763 |
Weak transcription Enhancers Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
6 |
nsv553597 |
chr11:18097481-18100022 |
Weak transcription Strong transcription Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
7 |
esv3479263 |
chr11:18097510-18100502 |
Weak transcription Strong transcription Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
8 |
esv3479274 |
chr11:18097510-18100502 |
Strong transcription Weak transcription Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
9 |
esv16818 |
chr11:18097605-18100066 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
10 |
nsv553600 |
chr11:18098635-18099639 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
11 |
nsv553601 |
chr11:18098635-18099763 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
12 |
nsv553602 |
chr11:18098635-18099827 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
13 |
nsv553603 |
chr11:18098635-18099968 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
14 |
nsv553604 |
chr11:18098635-18100022 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
15 |
nsv553605 |
chr11:18098635-18102232 |
Strong transcription Weak transcription Genic enhancers Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
16 |
nsv553606 |
chr11:18098635-18105302 |
Weak transcription Strong transcription Enhancers Genic enhancers
|
TF binding regionChromatin interactive region
|
2 gene(s)
|
inside rSNPs
|
diseases
|
17 |
nsv553608 |
chr11:18098688-18099639 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
18 |
nsv553609 |
chr11:18098688-18099763 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
19 |
nsv553610 |
chr11:18098688-18099968 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
20 |
nsv553611 |
chr11:18098688-18100022 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
21 |
nsv553612 |
chr11:18098688-18102232 |
Strong transcription Weak transcription Genic enhancers Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
22 |
nsv553614 |
chr11:18098785-18099639 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
23 |
nsv553615 |
chr11:18098785-18099827 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
24 |
nsv553616 |
chr11:18098785-18099968 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
25 |
nsv553617 |
chr11:18098785-18100022 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
26 |
nsv553618 |
chr11:18098785-18102232 |
Strong transcription Weak transcription Genic enhancers Enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
27 |
nsv553619 |
chr11:18098837-18099639 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
28 |
nsv553620 |
chr11:18098837-18099763 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
29 |
nsv553621 |
chr11:18098837-18099968 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
30 |
nsv553622 |
chr11:18098932-18099763 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
31 |
nsv553623 |
chr11:18098932-18099827 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
32 |
nsv553624 |
chr11:18098932-18099968 |
Strong transcription Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
33 |
nsv553625 |
chr11:18098932-18100022 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
34 |
nsv553626 |
chr11:18098932-18102232 |
Weak transcription Strong transcription Enhancers Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
35 |
nsv553627 |
chr11:18098983-18099968 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
36 |
nsv553628 |
chr11:18098983-18100022 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
37 |
nsv553629 |
chr11:18098983-18102232 |
Strong transcription Weak transcription Enhancers Genic enhancers
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
38 |
nsv553630 |
chr11:18099157-18099968 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
39 |
nsv553631 |
chr11:18099157-18100022 |
Strong transcription Weak transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
40 |
nsv553632 |
chr11:18099211-18100022 |
Weak transcription Strong transcription
|
Chromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|