Tag | Content |
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EnhancerAtlas ID | HS101-28938 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:38503120-38503850 |
Target genes | Number: 29 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr22:38503260-38503273 | GGGGACAGCTGCT | - | 7.04 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28205 | chr22:38503175-38509317 | Fetal_Intestine | SE_29187 | chr22:38503057-38509293 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CCAAGGTCAC AAAACTAGTC ACTGGTGAAG CTGGGCTTTG AACCCACCAC GAGCTAAGAA 60 CGGACAGAAT CATCTGTTGG AGTCCAGGGG GAGGGGTGAC TGGACTTGCC CCAGGGAGTC 120 AGAGGAGGCT TTGGGAAGGA GGGGACAGCT GCTTCCCAAC TGGACGGCAG GGGGAGGGAC 180 CGGTGGCTCT AGGCTGAGAG GACAGCAGGA CAGCAGCCCC GCAGCGGGGA CACCAGCAGA 240 GGGCCCACTC TTCCGGGGGG CTGGGCTGTG TTGGGGGTGT CAGGAGAAGC TGCTGGATCG 300 ACAGAGCCAG GGACCCCTCA CTGAGAAGCC TGTGTTCAGT TCTACGGGCA GTGGGGCCGT 360 GGAACGGTTC TGCTCCTGGG AGTGACATGG TCAGGTCCAT GTGGCTGCTC CCTGGGAGGC 420 TGCAGTGAGG AGGGCTGCAG TGAAAGGACC TTTCTCTTCC TTGGGCCTCC ATTCACTCTG 480 GCATCTCAGG CAATGACTAG CTCTTTGAGA CTCAGTTTCT TCCTCTATAA AATGGAGGCA 540 GAAATGCCAC CAGCCTCCTA GGGCTGCTAG AGGCTTGAAC GACTATTGCA GGGAACCGTG 600 CCCCACAGAG CCGGGTGCTG GGAAGGGCAG CCACGGTCAT CCTCCCTGGG AAGGGCATCT 660 GGTAGGCTGG GCCCTCTCCT TGGAACATAG CCCACTTTCC TCGAGTGACC CCTCCAGGCC 720 CTGGGGCCTG 730
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