| Tag | Content |
|---|
EnhancerAtlas ID | HS158-59349 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr9:139022060-139023130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr9:139022590-139022602 | GCCCACGTGGCC | + | 6.27 | | MYCN | MA0104.4 | chr9:139022590-139022602 | GCCCACGTGGCC | - | 6.27 | | ZBTB18 | MA0698.1 | chr9:139022379-139022392 | CTTCCAGATGTTT | + | 6.46 | | ZEB1 | MA0103.3 | chr9:139023002-139023013 | GGGCAGGTGGG | - | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_42022 | chr9:139021925-139024446 | LNCaP | | SE_63238 | chr9:138991973-139023521 | GLC16 | | SE_65568 | chr9:139021862-139023203 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I136130 | chr9 | 139022359 | 139026447 |
|
Enhancer Sequence | CTCCATTCGA CTTTCTGTCT CTGTGGCTCT GAGGGCCCTG AGCAGAATCA CAGGGTCTGT 60
CCTTATTCAT CCTGCCTCTC TTGCATTCAG GCTGGAAGCA TGCCATGCCT CTGCGGTCAG 120
GTAACTGAGG CCTGGAGCTC CTTCCACAGC AGAGCACAGA CGTCCTCACC CACCTGCACA 180
GCTGCGTGGC TCTCCCTGGG GGGATGGACA GGGAGGCTGT GGCGTCCCTG CTTGGCTGTT 240
CAGGTACCTG CAGTGTCAAC GCCTTTCCAA CTGTGATCTG TCCCCTCCCC GCATCACACC 300
CCACAGCGCT GGCCCAATCC TTCCAGATGT TTCCACAGGT CCTCCTGCAG TTGCCTCCCA 360
CTCAGAGGGA ACCTTCTCAA AGGCAAGCCT GACCCACAGG CAGGAGTCCG AGCTCCTTTC 420
TGAGCATCTG GAGACTCTAG CTTGGCCCAG TCATGGCTGA GGCCACCCTG TCCCGAGGAC 480
ACCAGGCTGT CCGTGGCCAG GGACCACACC CCCGACGCCC CTGAACCTTT GCCCACGTGG 540
CCCCCTGCAC CCCCTTCTTG GCAGTCTCGC ATACCTTTGC GAACTTTTCC TTTCATGTCC 600
TTCAAAATTC AGCTCAAGGC CTCCTCTTCC AGGAAGCCTT GCTGATTGTG GGCCGGACTC 660
ACCCCAGTGC CTGTCCCACA ACCGGCCCCA GGGAGGGAGG GGCTGTCTGT TTGCACACCT 720
GTCACCCGCT GCGTCACGTG CTCTCTTCAG GCAGGGCTGA CCTGGTTGGA ATGAGAGAAA 780
CGCTCTCCAG GCATCTCTGA CAAAAGGTTC TTGGCAACCG TGCTGTCTTG GTTGTCCTGG 840
GGCAGGTCCT TGCCTCTGAT TGCTCTGTCC TCTGTCCTGG CAGCAGTCCT GGACACCAAG 900
GCCAGGCTGG ACCTACCTCT AGGAGTGCTC TAGTAGGGAA TGGGGCAGGT GGGGGTCTAC 960
GAGGAGGCCA AACAGGGATC AGGAGGGCGG AGGGCGGAGG GCGGGCCCGG GAGAGAGCTC 1020
TCCCTGCAAC CTGGGGTGTG GGCCAGGGGC CTGTGTGAGA GCAAACCTCG 1070
|
