Tag | Content |
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EnhancerAtlas ID | HS183-10889 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr8:22473760-22474930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr8:22474606-22474621 | TGAACTCCTGACCTC | - | 6.22 | PBX1 | MA0070.1 | chr8:22474678-22474690 | CTATCAATCAAA | + | 6.18 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65795 | chr8:22474435-22481726 | Pancreatic_islets |
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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 | GGTGAGTACC CTGCCACCTC GGGCTGTCAT AGTGCTTACC GTGACCGCGC ACCTTTACCC 60 CGGGCTCTGT TCCGAGCGCT TCCTGTGCCT TAGCTCATTC CCTGCACCCT TGCTCGGCAT 120 GGACTGAGGC CGCACAGCTA GTAAGTAGCA CACCTAGTGC AAGGGAAGGT GGCGCAGAGT 180 GCAGGGAGCA TGGCTGAGCA GCCTGACAGC ACAGAAACCC TTGTCACTGA GAACGCTTGG 240 CAGAGTGGGG TGCTTTGATT GCCTGATGGT TAACTAGAAA ATTTTGTAGG CCGGGCGCTG 300 TAGCTCACCC CTGTAATCCC AGCACTTTGG GAGACCGAGG TGGGCAGATC ATGAGGTCAG 360 GAGTTTGAGA CCAGCCTGGC CAATATAGTG AAACGCCGTC TCTACTAAAA ATACAAAAAT 420 TAGCCGGGTG TGGTGGTGCA TGCCTGTTTT CTCAGCTACT CGGGAGGCTG AGGCAGGAGA 480 ATCGCTTGAA CCCGGGAGGC GGAGGTTGCA GTGAGCCGAG GTCGCGCCAC TGCAGTCCAG 540 CCTGGGCGAG AGAGTAAGAC TCTCTGTCTC AAAAAAGAAA AAAAAAGATT TGTAAACCTT 600 TTCTAAAATA CTAGTCTGCT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTG GGGAGATGGA 660 GTCTTGCTCT GTCACCCAGG CTGAAGTGCA GTGGCGCAAC CTCGGCTCAC TGCAACCTCT 720 GCCTCCCAGG TTCAAACGAT TCTCCTGCCT CAGCCTCTCT CCAGTAGGTG GGATTACAGG 780 CACCTACCAC CATGCCCAGC TAATTTTTGT AGAGATGGGG TTTCACCATG TTGGCCTGGC 840 TGGTCTTGAA CTCCTGACCT CAGGAGTGCT GGGATTACAG GTGTGAGCCA CCATGGCCAG 900 CTGCTGCTTG TTTAAATACT ATCAATCAAA TGAATGTAAT TTCTTCTGGG ACCAAGATCA 960 ACTCCTGAGG AAAAAAGCCC AGGTGTCTGG CGATGCCCTG GCATGCTCTG AATCCCACTT 1020 AATGAAATTA AATACATGAA ATGAGACGGT ATCTGTAGAG CCCTCCATAC AGTGCCTGGG 1080 GCATAGTTGA TACTCAGGTG TCAGCCATGC TTACTATTGG TAATTATGGT AACTGCCTGC 1140 CTTTTCCTTA TAACCTTTGT CTGCCTCTGT 1170
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