| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16047 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:26225650-26226250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr2:26225910-26225921 | GCTTCCCGCCC | - | 6.02 | | MYC | MA0147.3 | chr2:26226011-26226023 | GACCACGTGCCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_09566 | chr2:26223930-26226896 | CD14 | | SE_26712 | chr2:26222093-26229700 | Esophagus | | SE_32014 | chr2:26225382-26226456 | Gastric | | SE_35193 | chr2:26223909-26226117 | HeLa | | SE_64640 | chr2:26224712-26226240 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 26226012 | 26226104 | | chr2 | 26225947 | 26226220 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I025999 | chr2 | 26222672 | 26226868 |
|
Enhancer Sequence | CCTGAAAGGA GGAACCCCAA AGAGAATGCC ATTGGCCAGT AAGGCCTTCT GTCATCCTCA 60
TCCGGCATTG CTCATTCTCT GAACTTGACC TTGTTGTTTC CCCTTCCCAA ATGAAAATCA 120
GTCTCTTCTT TTGCTATCCT TGAACACACA TCCTACGCCT TGCTGACCCC AGGCCTGGGG 180
TGACCGGGGT CCTCCTTCAC CCAGTTCATG GCCTGGAGAC TCTTTGGATG CCCTGTCCAG 240
CTGGCATGCC CTGCTCAGCA GCTTCCCGCC CCACAGGATT CTCAGGGCAC TCCAGCTTCT 300
GCCAGGTCTG CCCTCCCTAC ACGGAAGCAG AAGAAACAGA TGCAGAGAAG AACAGAAGGA 360
AGACCACGTG CCCTGAAGTT ACAGAGGGAG GAGCTTCCAG TTTGGACTTT CCAGTTCCCC 420
ATCTTGAGCT AGCATGAATA GGCTTCTGCT GCTTCCAACC AGATGATGCC AGACTCACAG 480
CTTGGACTTG ATTTGATTTG AACCAATTCA AAATGTAGCC ACCACCCACC TTAATATCCC 540
TACCCTAGAC CGGCCTCTCA CTCCCAATTA CCCTGTTCCT GTCACCATCA CCAGCATTTG 600
|
