Tag | Content |
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EnhancerAtlas ID | HS184-08713 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:121998240-121999300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr12:121999214-121999227 | TTCTGGAACCTTC | + | 6.33 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58854 | chr12:121951240-122029731 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I121559 | chr12 | 121997895 | 121999100 |
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Enhancer Sequence | TTGTGTGTAA AGGCAGGAAG AAACTGACTT TATACTTTTT CTTTCCTTCA CCACAGAACC 60 CCTTCTTCAA ACAGAAGCTT TGATGACAGC CAAATACACA TAAATAAAAA CAAAACAAGC 120 AGCTCAGGCT GATGCAGGAG GTGGGTGGGG GGTGCTCAGA ATTCAGACCT AGATCCCTGG 180 GGTTTCCCTT TGAAATTCAC TGGGTTGGGG CATTTTTGGG TCCTTTCCCA GGGGCGAGGC 240 ACTGAGTTTC AGTTCCTGAA TACTCGGATC ACTTCCCTTA AATGTATAAA GTGGGCAGGG 300 GCAGGGGCAG TGGGGGCAGA GGAAGAGACG GGGGCCGCCA GTCCCTTTTG GCCTGAGCTG 360 AGAGATGAAG AATGAGCCCT CCAGCCTCCC GGTCTGATCT GCCACAGGAG CAAAGGGAAC 420 CAGGCACACA GGCTGAGTCT CTAAGCAAGA GGTTTGGCAC CGGGGAGGAG GCAGGTAGCC 480 TAAAGGGATG GAGGGGACAG ATCAGTGCCA AGAATGGAAT GCAGCCCTCC CAGCCTTTAG 540 GAGCAGCCAT CCCTAGAGCA GCTGACAGGG ACAAGCGTCC CTTCAGACCT GCAAGGGATC 600 CACACTGCTG GGGCTCTCGG GTTCCTGAAG TCAGTGGGTT ACAGGAGAAA TTTTCCACAT 660 GGGGCAGTGC CTGGAGTTCC TAGGCAGGCC AGCAGCCTCC CTCCCTCCGC CGCCCACCCA 720 CCCCAGGATC ATCGGTGTTC TGGCTCCCGG GCTGCACACA CATCCAACAG GTTCCAGCTG 780 CGGAAATTAG TCCATGGCCC TGTGGCCCCT GCTTTGAAGG TTCCATCCGT CAGCTCCGAA 840 AGCCTCGGGC TCGGGGCCAG GACGAGGCTG CTGAAAGTCA TCTTGAAGGC TAATGTGAAA 900 CATACACGGG CGCGACCCCA AACTCCCCAG AGCCCGGCTC TTCCGAGAGC TCACAGAACT 960 CTTCCACATC ACAGTTCTGG AACCTTCTCC AGCATCCTCA CATTTCTGGA CTGGTTTTGT 1020 ATTTTGTTCC TCATCCGTGT CACACAGGTA GCACTGATTA 1060
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