| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07652 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:53297060-53298440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:53297631-53297651 | CCCCACCCCAGCCCACCCCA | + | 6.18 | | RREB1 | MA0073.1 | chr12:53297641-53297661 | GCCCACCCCACCCCACCCCA | + | 6.1 | | RREB1 | MA0073.1 | chr12:53297645-53297665 | ACCCCACCCCACCCCACCCC | + | 6.22 | | RREB1 | MA0073.1 | chr12:53297650-53297670 | ACCCCACCCCACCCCACCCA | + | 6.22 | | RREB1 | MA0073.1 | chr12:53297651-53297671 | CCCCACCCCACCCCACCCAC | + | 6.67 | | RREB1 | MA0073.1 | chr12:53297636-53297656 | CCCCAGCCCACCCCACCCCA | + | 6.8 | | RREB1 | MA0073.1 | chr12:53297646-53297666 | CCCCACCCCACCCCACCCCA | + | 7.67 | | RREB1 | MA0073.1 | chr12:53297656-53297676 | CCCCACCCCACCCACACCGC | + | 7.67 | | ZNF143 | MA0088.2 | chr12:53297301-53297317 | TTCCCACAATGCCTCC | + | 6.01 |
|
| | Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
| SE_23067 | chr12:53293079-53302882 | Colon_Crypt_1 | | SE_23787 | chr12:53296755-53298845 | Colon_Crypt_2 | | SE_24992 | chr12:53296540-53299679 | Colon_Crypt_3 | | SE_27647 | chr12:53288696-53303037 | Fetal_Intestine | | SE_28539 | chr12:53288457-53303256 | Fetal_Intestine_Large | | SE_31746 | chr12:53295793-53302843 | Gastric | | SE_34646 | chr12:53296478-53303608 | HeLa | | SE_43420 | chr12:53296705-53297615 | MCF-7 | | SE_43420 | chr12:53297676-53298740 | MCF-7 | | SE_47304 | chr12:53292933-53302628 | Panc1 | | SE_47563 | chr12:53297064-53298856 | Pancreas | | SE_50235 | chr12:53293003-53302879 | Sigmoid_Colon | | SE_52377 | chr12:53291888-53302844 | Small_Intestine | | SE_56763 | chr12:53296731-53299669 | VACO_400 | | SE_57363 | chr12:53297031-53298834 | VACO_503 | | SE_57922 | chr12:53296950-53298736 | VACO_9m | | SE_65517 | chr12:53295161-53302467 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATAGATGAGG AAATAAGACT TGGCAAGGGA GTCCATAACC AGGAACCGGC AGAGCAGTGC 60
GAACCAAGAA TTCAGATTCC AAAGCCTATG CTTAGCTGCT CTCTATAAGG ACCCCAGGGC 120
TAGCAAAACG CAGTCAACAA GTCAAGTCCA GGCGCTTGGA GCGCCAAGGG CCCCCGACCA 180
CTGGGTTCCT GGGGCTCCGG TTCCTCCCGG CTTACTCTGC CCCAGGATTT CCCTCCTCCC 240
GTTCCCACAA TGCCTCCCAG GAGCCAGTCA GCGTGAAGGG CCCAATCCTC GGGGCCGCCG 300
GGGGCCCGGG GCCCCTCAGG CAGCGGAGTC CCAGGGCTGC AAAACCCGGC CTGGCTCCTG 360
CTGTGTGAAA GTGGAGCCAG GCCGCTGGGG CGGAGCAGGG ACAGGACGCG AGAAAGGGAC 420
ACGGGCTGAA TGGGCGAGGG GCGTTGGTGG GCGACCGCGT TATCTGAAGC CATAAACTTA 480
ACAGGACGTA AACCCCGGGC GGGGCGTCCC ACGCCCGCAG ACTTTGAATC CTGCATGGGC 540
TTTCCGAGGC CAGGCCCTGG CGCCTCCTCC ACCCCACCCC AGCCCACCCC ACCCCACCCC 600
ACCCCACCCA CACCGCCCCC GACGCCGAGC TCCGCCAGGT GGAGGAGAGC GTCCCGAGAC 660
TGCTGCCCGC AGCCCCTCAC CCCGCCCTCG GCCCCGCCCA CGCTGCCGGC GCAGGGGCCG 720
GGGTATGACT CATTCTGTGA CCCCCGCACT CAGGCCTCCG GGCGCCAAAG GCCTCAATCA 780
ATATTTGCCC GTTTGAACCG AGACACCCAC TTCCTTCTCC TAGAATGCTA GAATCACACC 840
AAACCCCTAT GTAAAAAAAA GAAAAGAAAG AAAAAAAATC ACAAAGGCAC CACTGGGGAG 900
CCCTTGGGGT AGTGCTGGCG AAGAGGCGAA CCTGGAGGAG GGTAGTCCCC GAACAGCTGG 960
GACTGCCGCA GGGCGATAGC TTAAAAGACG GTCAGAACTC GGGTTGGGGT GAGAACAATA 1020
ACCGCTATTA TTTTTTATAA TTTGGGGACA GAATGACCTG AGGAAGAACG GGATTTGTAG 1080
AGAGGGGTGG TGGGAACTAG GCTGTACCCT TAAGTTGTCT CTCTCTTCCA AGACCCTCCA 1140
GTTTAAAAGG GAAGAAGGAA GCCCCAGGAT TCATCCCGGC TGTCCAGACC CTCTCCCCAC 1200
CCTCACCCAG CCCAAACCAA GGTGCACGGG AGGGGTGAGT CGGAGGATGG AAGGGAGAGT 1260
GTCGCCAGGG CGGGTGAGGC CCAGCAGGAC GCCAGCTGGG GGCTGGAGAT GTGCATAGGG 1320
ACCGGGACTA CCAGGAGAAA GGGGCTGCGG GCACAGTCAG CCACGCAGGG GGGACCCTCA 1380
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