| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv885900 |
chr6:54517968-54852462 |
Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
13 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv5309 |
chr6:54834971-54855729 |
Enhancers Active TSS Flanking Active TSS Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
nsv603134 |
chr6:54841672-54851340 |
Enhancers Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv20291 |
chr6:54846098-54851665 |
Weak transcription Enhancers Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3474002 |
chr6:54846245-54851547 |
Weak transcription Enhancers Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv3474003 |
chr6:54846291-54851530 |
Enhancers Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv3474001 |
chr6:54846368-54851443 |
Weak transcription Enhancers Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv499725 |
chr6:54846381-54851446 |
Enhancers Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3474004 |
chr6:54846382-54851446 |
Enhancers Weak transcription Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv603135 |
chr6:54848142-54849779 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
nsv603136 |
chr6:54848142-54849908 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv603137 |
chr6:54848142-54850370 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv603138 |
chr6:54848142-54850396 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv603139 |
chr6:54848142-54851038 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv603140 |
chr6:54848142-54851340 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
nsv603141 |
chr6:54848142-54852462 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
nsv603142 |
chr6:54848265-54849908 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv603143 |
chr6:54848265-54850139 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv603144 |
chr6:54848265-54850396 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv603145 |
chr6:54848265-54850977 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv603146 |
chr6:54848265-54851340 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
nsv603147 |
chr6:54848265-54852462 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
nsv603148 |
chr6:54848317-54849908 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
nsv603149 |
chr6:54848317-54850396 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
nsv603150 |
chr6:54848317-54851038 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
nsv603151 |
chr6:54848317-54851340 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
nsv603152 |
chr6:54848414-54849908 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
nsv603153 |
chr6:54848414-54850139 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
nsv603154 |
chr6:54848414-54850396 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 30 |
nsv603155 |
chr6:54848414-54850977 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 31 |
nsv603156 |
chr6:54848414-54851340 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 32 |
nsv441998 |
chr6:54848455-54850142 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 33 |
nsv603157 |
chr6:54848810-54850396 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 34 |
nsv603158 |
chr6:54848810-54851340 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 35 |
nsv603159 |
chr6:54849019-54850977 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 36 |
nsv603160 |
chr6:54849161-54851340 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 37 |
nsv603161 |
chr6:54849271-54851340 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page:
1
