| Tag | Content |
|---|
EnhancerAtlas ID | HS012-04517 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:75040880-75042150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:75041401-75041421 | CCCCACCCCACCCCATAACA | + | 6.79 | | RREB1 | MA0073.1 | chr11:75041411-75041431 | CCCCATAACACCCCACACCA | + | 7.01 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_03287 | chr11:75041374-75041920 | Brain_Angular_Gyrus | | SE_04031 | chr11:75040313-75041841 | Brain_Anterior_Caudate | | SE_04951 | chr11:75038698-75042281 | Brain_Cingulate_Gyrus | | SE_05927 | chr11:75039003-75042234 | Brain_Hippocampus_Middle | | SE_07907 | chr11:75038776-75042175 | Brain_Inferior_Temporal_Lobe | | SE_09621 | chr11:75038907-75042083 | CD14 | | SE_13044 | chr11:75040931-75042114 | CD34_Primary_RO01480 | | SE_13386 | chr11:75038965-75042257 | CD34_Primary_RO01536 | | SE_14290 | chr11:75039890-75042323 | CD34_Primary_RO01549 | | SE_23271 | chr11:75039239-75042140 | Colon_Crypt_1 | | SE_24003 | chr11:75041047-75041451 | Colon_Crypt_2 | | SE_24003 | chr11:75041600-75042140 | Colon_Crypt_2 | | SE_25192 | chr11:75039037-75042197 | Colon_Crypt_3 | | SE_25898 | chr11:75038978-75042365 | Duodenum_Smooth_Muscle | | SE_26962 | chr11:75041074-75042209 | Esophagus | | SE_28109 | chr11:75039189-75042419 | Fetal_Intestine | | SE_29208 | chr11:75039169-75042452 | Fetal_Intestine_Large | | SE_31429 | chr11:75039234-75042571 | Gastric | | SE_41608 | chr11:75041068-75041957 | LNCaP | | SE_42220 | chr11:75039229-75042237 | Lung | | SE_47208 | chr11:75032345-75042889 | Panc1 | | SE_49998 | chr11:75038987-75042142 | RPMI-8402 | | SE_50175 | chr11:75039169-75042236 | Sigmoid_Colon | | SE_52494 | chr11:75039154-75042185 | Small_Intestine | | SE_54712 | chr11:75038901-75042420 | Stomach_Smooth_Muscle | | SE_59773 | chr11:75038940-75077709 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr11 | 75041227 | 75041400 | | chr11 | 75041400 | 75041600 | | chr11 | 75041361 | 75041638 | | chr11 | 75041069 | 75041957 |
|
Enhancer Sequence | TTTAAAATCT ACCCAGGCAT GGTAGCACAT ACCTGTGCTA CAAGTCTCAG CTACTTGAAA 60
AGCTGATGCA GGAGGATCAC TTGACCCCAG GAGTTCGAGG CTGCAGTGAG ATGTGATTGC 120
ACCACTGCAC TCTAGCCTGA ATGACAAGAC TGAGACCCTG TCTCTAAAAA AAAAAAAAGT 180
CACTACTGCC TCTCAGACTC CCTTTCACAC ATGACAGAGG CCTGACAAAT TTGCACTGAA 240
TGAATAAATG AACGAACGAA CAATCTGTCA CTCATTTCCC AACTTCTAGC CTCTCTCTTC 300
TAGTCTATTT ACCTACACAG CTGCCACGTG AACCTTCAGA TCCTGCTGCT CCTGCAAGCT 360
GTGTGTTCAG ACAAATTGCT GAACTTAGCT GAGCCTTCAA TTCCTCAACT ACAAACAGGG 420
ACTCTACTTG GGTAATTAGG AAGATTGAAA GAAAGCATAA GCACAGCATC TCAAGGGCTA 480
AGGAGGAGTC CAGGAAAAGC TGTTGAAGGA AAGCTGTTTC TCCCCACCCC ACCCCATAAC 540
ACCCCACACC ACCCTGATCC TCTAATCTCT CTGTTCCAAA GGCTGCAGGA AAGAGCCCAG 600
CCCCTGGGCT GGCCCCTGGC TATATGTAAA TGTTTATGCC AAGCCCAGCC TCCTAAGGAC 660
AAGTTATTTG CTTTGCTTGT AATTAATTGC AGAAGGCCTG CCTGGGTAAT AAACTCTGCC 720
GAAGAAATAT AAACAGTTTG CACAGAGCTT CAAATCCATT GTGAGGCCAA GAGAAAGGGT 780
CTGCTAGGAA TGGAATGTTC TCCCCAGTCT TCCTCTAAGC TGGAGGCAGA GAGATCACTG 840
AAGGTCAGAA CTGAGAGGAC CCTTGGAAAT CATTTGAAAA ATAGCACCTG GCATCATGAC 900
CTTGTTCCAG GCCCGGCTGA GCACTTGCTT TATATGGTAC AGCTATTTTC CCATTCTAAA 960
GATGAAGAAA CTGAAGCTGA ATGAAAGTGG CAGGGAACTT TCCCCAACTA GAAGGCAGCT 1020
GGGCTGAAAG TTGAATCTGG CTGGACTTTA GAGAAAAAGA AAGACAGCCA TTCATTCAAC 1080
AAAAATATCC CGTGTCCCCC GTGCCAGACA CTGGTACCTG GTGACACAGC TCCTGCAGCA 1140
CTTGCATTCC AGCAGGGAGA GGCATATTTC AGATGTTGAG GACTAAAATC TGATTTTTAT 1200
TTTTTGAGGC GGAGTCTCGC TCTGTCGCCC AGTGGCGCGA TCTCGGCTTA CCGCAACCTC 1260
CGCCTCCCAG 1270
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