| Tag | Content |
|---|
EnhancerAtlas ID | HS012-22594 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:22439040-22440200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr8:22439388-22439399 | CTTCTGGGAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_26744 | chr8:22431344-22440146 | Esophagus | | SE_27805 | chr8:22435253-22440231 | Fetal_Intestine | | SE_28771 | chr8:22435400-22440426 | Fetal_Intestine_Large | | SE_35195 | chr8:22438862-22441354 | HeLa | | SE_52777 | chr8:22435698-22440170 | Small_Intestine | | SE_54062 | chr8:22427620-22440243 | Spleen | | SE_57572 | chr8:22436025-22439554 | VACO_503 | | SE_57572 | chr8:22439848-22440142 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCGGTAGGGC CTCCCGCTCT GCAGAGCCTG TGGCATTCCC CCTCCTCCAC CACCCCACGT 60
ATTGAGCAGC CCTTGCTCCT GCCCATGGGC TAGAGCTCAG CCCTAAAGCG GCCTTCTTGG 120
GCCCTCTCCA CACCTTGGTG AGAAGGTCCT GGGCTCTGCT TCCTGCAGCA GGGTGGGCTG 180
AGGGGTGTTC CCATGCCTGG TTGGGTAAAG GTGGGCGCCA GGCTGGGCGT GCAGTCACAG 240
GCTGGGCAGG GCGAGCTGGC ACCAGCCACC TTGAAGCCCG GGTTTGACTG GTTCCCAAGA 300
GTGTGCAGGG CACAGGGCGT GGGCATGAAG TGGGTTGAAG AGGGGAACCT TCTGGGAAAG 360
GTATGCCCGA GGCTGCATCC CCAGGACTCC TGCTTCCAAC AGGGCATGGC CTTTGTTTAG 420
TTCCCAGCTG GAAGTGAGGA CTTGGGGGGC TCATTCCTCA TAGAGGCTGT CTGTTCCTCC 480
CCATCACTGA AGGCAGATGC CCGATCCTGG GTTACTCCTA GGGTTTTGAG CCTATAAGCC 540
AAGGTGGGGC CAGGGTGGGG CCTGGAGGCC AAGCTATAGG GGGAACAGGT GGCTCCCTGG 600
GGTGGGGCAT TGCAGTGAGT CACAGATCGG GAATGCCAGG AGATCCCCGA GCCAGGAGAG 660
CCCTCTGCAC GGGCCTAGAA CCTGAGTCAG ACACCTCTTG CATCCTGGCC ACCCCCACAT 720
TGTCCTGCTC TCTTCAGCCC TACCAAGCCC CTCCTTCTCC AACTGCCCTG CCCTGTGGTG 780
TGGCAGAAGC CGGCTCCCTT CATGTCATTC AGGTCCCTGG GTGTTTGCAG GAGCGGGACC 840
CCAAGAAGGA GGGTAGAGAG CACCTCATGG CATCTGGGAA TGGGGCAGAA AGCTACAGGA 900
GGCTGAGGGT CTGGCAGCGG AAGGGCAGGA GCCTCGGACT GTCTCTTCCT CTGGGGTTCT 960
CTGGAGGGAC CAGGGCTCGG GGGAGGTAGG CCTGGGCTGT AAGTCAGGCC TCTGGTTCTG 1020
CACCAGGCAA GCCCAGACTC CAGTCTCTTA ATTTTTTTTT TTTTTTTTTT TTTGAGACAG 1080
AGTCTCGCTC TGTTGCCAGG CTGGAGTGCA GTAGCGTGAT CTCGGCTCAC TGCCACCTCT 1140
GCCTCCCGGG TTCAAGAGAG 1160
|
