| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02338 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:207174820-207175550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr1:207175391-207175402 | AACTTCCGGGT | - | 6.14 | | TFAP2A | MA0003.3 | chr1:207175303-207175314 | TGCCTGAGGCA | - | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_26663 | chr1:207174076-207177334 | Esophagus | | SE_27711 | chr1:207174549-207176229 | Fetal_Intestine | | SE_31518 | chr1:207174225-207175679 | Gastric | | SE_33873 | chr1:207174470-207177225 | HCC1954 | | SE_34694 | chr1:207175413-207177474 | HeLa | | SE_57640 | chr1:207174392-207175686 | VACO_503 | | SE_57951 | chr1:207174806-207175106 | VACO_9m | | SE_57951 | chr1:207175382-207175652 | VACO_9m |
|
| | 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 |
| GH01I207001 | chr1 | 207174816 | 207177209 |
|
Enhancer Sequence | GGTCTTATCT CAGGAGCACT GGGCTGGTGG AAGAGATGGT GATTGTTATC AGATGGCATG 60
ATGGTGACAG TGAGGGGAGG CAGACCCAGG GCTTGAGAAG GACAGAGGAC AGGTGAGCAT 120
TTCCTCACCC AGGACAGGCC AGACGTGCTC CCTGAACTGT TGCCTGTGCT GGGTGTTTGC 180
CATCAGCCAT TTTTCCCTCT GATTTTATCA CTTCCAATAT AGGTATGTGC ATTAATGTAG 240
GTATGTGCAT TCTTAGAGAT TCATTCCTTT GGCTTACACT AACGACTTTT CTTACACAAA 300
AGACCTCAGT GAACCTTGGG AGAGAAGGCA GTTCTTGGGG AGGAGAAAGA TTGAGACTGG 360
GAAGGCACAT GTAGCTGCTT TGTATTCTAC CCTCTGGTTG GCCTTAGTGC CCTCTTTTTG 420
CTTGGTCTCT GGGCACTGAA TCCTTCTAGG AATCTTCTTA GTTTTAGGCA CTGGTTTTAA 480
TCCTGCCTGA GGCAGTTGCA ACCACCTTTT CTGAGCTAAC AACAATCTCC ACCCCCTTAC 540
CTAGGAAGCA CCTGCAACTT TAGTCAGATG GAACTTCCGG GTGTCTCACC TGGGAGAGAG 600
AGCTATGTAG CCCTTAGGAG GAGTTCAGTG TTGTTAACCT AGTGCAGCAG AATTGTGAGC 660
GGGGCTGAGC CTCTGCCTCA GCCTCAACTC CATTGGGGCT GCGGACAGGA GGGAAAATTG 720
GGGGTGGGGA 730
|
