| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18962 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr4:6955380-6956260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr4:6955900-6955910 | GGGGCGGGGC | - | 6.02 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_01116 | chr4:6955332-6956446 | Adrenal_Gland | | SE_23500 | chr4:6955378-6956349 | Colon_Crypt_1 | | SE_24085 | chr4:6955378-6955879 | Colon_Crypt_2 | | SE_24085 | chr4:6955899-6956345 | Colon_Crypt_2 | | SE_27664 | chr4:6955650-6956461 | Fetal_Intestine | | SE_28549 | chr4:6955294-6956423 | Fetal_Intestine_Large | | SE_31576 | chr4:6955301-6960712 | Gastric | | SE_43280 | chr4:6955381-6956503 | Lung | | SE_50164 | chr4:6955289-6956405 | Sigmoid_Colon |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 6955458 | 6956236 | | chr4 | 6955494 | 6955889 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I006953 | chr4 | 6955357 | 6960529 |
|
Enhancer Sequence | ATAGATCAGT TTTGGGGGAC ATGAGGTTGT TAGTTAGCTC TGGGTTTTCG TTTTTGTCTT 60
CAACAGCATT TGAAGTGAGT GAGGGGGAAT CCAGAGCGAT GGTTCTAGTG TAGGTATTTG 120
GATTAATTTC ACGGTTCTGT GCTTGTGACT CAACGGCAGA CCTGGCCGCT GCTTCACAAG 180
GCACAGTGCC TGGCACACTG CAGACGCTCA GGAAGCGCTG TGTGCTTGGC GCTTTTCCAG 240
GTCCGAGGTC CCGGTGGGTT TTGTGACAGG TAGCCTGGAC GTGCTGTGTG CTTGGCGCTT 300
TTCCAGGTCC GAGGTCCCGG TGGGTTTTGT GCCTGGTAGC CTGCCCTGCC ACGGCATGTG 360
GTGCGGAGCC GTGTCCCAGG CCCGAGAACC CGTCACTCAG GCTTTGCTTC CCAGACTTTG 420
GGCTCACTCC TCCCTCCCTG TGACTGGGGA GGCCCGCCCT GCCGCCCCCG CCTTTCCGCC 480
GGCCTGCTGG GTCCAGCTTG CCTTCATCTG GCAGACGCGA GGGGCGGGGC TCCGAGTGCA 540
CCCATGGAGT TTCCCCGGGA CTGTGGCTCT GGCGTGCCAG GAATGCGGCA CGGGGAGAGT 600
CCGTGCTTCT GCAGCCGGCC CCTCGGAGCT GCGAGGTCAC AGTAGACATG ATGGCCATCT 660
CCCCTGCGCT CCTGTTCATG GACAGGTTTG TGGCTGCTTT CTTGCCTTTC TTGCTGTTGG 720
AACTGGAGAC TTAACTGGAA GCAGAGTCTT TCCTGCGTGT AGCTTTGACA GCATGTGACC 780
GTCGGCCTTG GTTGGGCTGA GGTGTTTCTG TGGGTCTCCC CCGGTGTGAA ATGGAGGTGA 840
TCCTTTCTAT CTAGGCAGCA TCTCTGAGTG CCCGAGCTCC 880
|
