No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
rs148902942 |
chr2:113879397-113879398 |
Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
2 |
rs571972871 |
chr2:113879429-113879430 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
3 |
rs143564427 |
chr2:113879499-113879500 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
4 |
rs180946470 |
chr2:113879536-113879537 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
5 |
rs148029333 |
chr2:113879551-113879552 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
6 |
rs186212321 |
chr2:113879559-113879560 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
7 |
rs191457069 |
chr2:113879570-113879571 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
8 |
rs529495026 |
chr2:113879597-113879598 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
9 |
rs544083060 |
chr2:113879621-113879622 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
10 |
rs563880378 |
chr2:113879638-113879639 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
11 |
rs1794065 |
chr2:113879733-113879734 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
LD-proxies of rSNPOverlapped rCNV
|
n/a
|
12 |
rs141716564 |
chr2:113879765-113879766 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
13 |
rs566150322 |
chr2:113879832-113879833 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
14 |
rs528517538 |
chr2:113879833-113879834 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
15 |
rs548176024 |
chr2:113879949-113879950 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
16 |
rs181480876 |
chr2:113879953-113879954 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
17 |
rs187162408 |
chr2:113879987-113879988 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
18 |
rs565670622 |
chr2:113879988-113879989 |
Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
19 |
rs529872811 |
chr2:113880012-113880013 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
20 |
rs191939727 |
chr2:113880015-113880016 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
21 |
rs4251990 |
chr2:113880017-113880018 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
22 |
rs538802435 |
chr2:113880026-113880027 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
23 |
rs560238153 |
chr2:113880027-113880028 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
Overlapped CNVs
|
n/a
|
24 |
rs4251991 |
chr2:113880049-113880050 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
LD-proxies of rSNPOverlapped rCNV
|
n/a
|
25 |
rs4251992 |
chr2:113880069-113880070 |
Weak transcription Enhancers Genic enhancers Bivalent Enhancer
|
Chromatin interactive region
|
1 gene(s)
|
LD-proxies of rSNPOverlapped rCNV
|
n/a
|
26 |
rs416778 |
chr2:113880231-113880232 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
Overlapped CNVs
|
n/a
|
27 |
rs416779 |
chr2:113880233-113880234 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
Overlapped CNVs
|
n/a
|
28 |
rs11575824 |
chr2:113880266-113880267 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
Overlapped CNVs
|
n/a
|
29 |
rs376561929 |
chr2:113880275-113880276 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
Overlapped CNVs
|
n/a
|
30 |
rs183411133 |
chr2:113880288-113880289 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
Overlapped CNVs
|
n/a
|
31 |
rs554606339 |
chr2:113880289-113880290 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
Overlapped CNVs
|
n/a
|
32 |
rs2853628 |
chr2:113880292-113880293 |
Weak transcription Enhancers Bivalent Enhancer
|
Chromatin interactive region
|
2 gene(s)
|
LD-proxies of rSNPOverlapped rCNV
|
n/a
|