Tag | Content |
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EnhancerAtlas ID | HS193-12536 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr16:27781340-27782330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr16:27782217-27782238 | TCCCTCTCCCCATCCTGCCCC | - | 6.76 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33736 | chr16:27774783-27785021 | H2171 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH16I027769 | chr16 | 27780511 | 27782536 |
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Enhancer Sequence | TGAGGAGAAA GTGGGCGCCA CACACAGCCC CTCCCGGCCC CTGGGCCCGC TTGCTTTGCA 60 AGTTGCTCTG ATGTACATTC CGAAAGGGTT TTGAAACGAT GATCAAACGC ATTGCTTTTC 120 AACTTAGTCA TTTTCTAAAG CTCAGCCAAG CCTCACCGGA AGCCTGTGGA ATGGACTTAC 180 CTTGTCTGGG GACATTTGGG TTTTTCACAG TCTGGAGTGC TGAAGATTTT AAATGCTTCA 240 TTGCGTTTCC TGCTGAGAAA AGAGGCTACA GCCTGCCTCC ATTCCAGAAA TGCCTGCCGG 300 CCAGTTTGGG GAAGGGCCTT CCTTCTCCCG TTTCTGTGTT CCTGATTTAG AAAGATTCAA 360 GGAGAAAAAT AGAGCTTAAT ATTTCATGGA TTCACTGGGA TTTCTCGGCC CCAGTCTCAG 420 CTGCATTAAG TTCATAACGA TTTGTAAATG CCACGTTAAG TTTACTCATT GAAACCCCCT 480 GATGTCCAAA CGCCAGAGGC CAAGCTCTTG AAACAAAATG AGTTTCCCTG CACTGTAGCG 540 GGGTTGGCTG GCTGGGCTGG TCACTAGGAA GTCATTTAAT TGTAACATTG CCCTTGAAAT 600 GGAAGAGAAC CAGGCTAGGG CTGGAGGGCA CTGACAGCGG ACCAGGGAGA GGGGCCCCGT 660 CAGGAGGGCC GTGGAGGAGA GGATCCTTCC CGAGGGCCAG CTGTGTGAAC ACTTTGATGT 720 GTCCTTTGGG AAATCCTTCC AGCCACCCTT TGACCTAGCC AGTATGATGC CCGTTTTACA 780 GATGTGGGAA CTGAGGCTCT GGCTGGTGGA GCCAGGTGCT GAAGATCATG AAGCCAAAGC 840 CATCAGGGCT GTGCCTGCCT TCCAGCCTCC TCTCACTTCC CTCTCCCCAT CCTGCCCCAG 900 ACTCCAGCCC TCTGGCCGCT TTCTGGGGCA AACACCAGCA GCCCAGTGAC TTCCCACCTT 960 GGGCCTTTGC TCTGCTGCTC CTCTGCGTGG 990
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