| Tag | Content |
|---|
EnhancerAtlas ID | HS101-46547 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr9:139022010-139023120 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
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 | GCTCTGTCCC CATGAAACAC TCACCCCCGT CCCCTCCCAG CCCCGGGACC CTCCATTCGA 60
CTTTCTGTCT CTGTGGCTCT GAGGGCCCTG AGCAGAATCA CAGGGTCTGT CCTTATTCAT 120
CCTGCCTCTC TTGCATTCAG GCTGGAAGCA TGCCATGCCT CTGCGGTCAG GTAACTGAGG 180
CCTGGAGCTC CTTCCACAGC AGAGCACAGA CGTCCTCACC CACCTGCACA GCTGCGTGGC 240
TCTCCCTGGG GGGATGGACA GGGAGGCTGT GGCGTCCCTG CTTGGCTGTT CAGGTACCTG 300
CAGTGTCAAC GCCTTTCCAA CTGTGATCTG TCCCCTCCCC GCATCACACC CCACAGCGCT 360
GGCCCAATCC TTCCAGATGT TTCCACAGGT CCTCCTGCAG TTGCCTCCCA CTCAGAGGGA 420
ACCTTCTCAA AGGCAAGCCT GACCCACAGG CAGGAGTCCG AGCTCCTTTC TGAGCATCTG 480
GAGACTCTAG CTTGGCCCAG TCATGGCTGA GGCCACCCTG TCCCGAGGAC ACCAGGCTGT 540
CCGTGGCCAG GGACCACACC CCCGACGCCC CTGAACCTTT GCCCACGTGG CCCCCTGCAC 600
CCCCTTCTTG GCAGTCTCGC ATACCTTTGC GAACTTTTCC TTTCATGTCC TTCAAAATTC 660
AGCTCAAGGC CTCCTCTTCC AGGAAGCCTT GCTGATTGTG GGCCGGACTC ACCCCAGTGC 720
CTGTCCCACA ACCGGCCCCA GGGAGGGAGG GGCTGTCTGT TTGCACACCT GTCACCCGCT 780
GCGTCACGTG CTCTCTTCAG GCAGGGCTGA CCTGGTTGGA ATGAGAGAAA CGCTCTCCAG 840
GCATCTCTGA CAAAAGGTTC TTGGCAACCG TGCTGTCTTG GTTGTCCTGG GGCAGGTCCT 900
TGCCTCTGAT TGCTCTGTCC TCTGTCCTGG CAGCAGTCCT GGACACCAAG GCCAGGCTGG 960
ACCTACCTCT AGGAGTGCTC TAGTAGGGAA TGGGGCAGGT GGGGGTCTAC GAGGAGGCCA 1020
AACAGGGATC AGGAGGGCGG AGGGCGGAGG GCGGGCCCGG GAGAGAGCTC TCCCTGCAAC 1080
CTGGGGTGTG GGCCAGGGGC CTGTGTGAGA 1110
|
