Tag | Content |
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EnhancerAtlas ID | HS141-01811 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:228999720-229000700 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr1:228999832-228999843 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr1:228999831-228999842 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr1:228999832-228999842 | TCAAGGTCAT | + | 6.02 | Myog | MA0500.1 | chr1:228999784-228999795 | CTGCAGCTGTT | - | 6.02 | RREB1 | MA0073.1 | chr1:228999739-228999759 | GTGTTGGGGGTGGGGTGTGT | - | 6.16 | RREB1 | MA0073.1 | chr1:228999730-228999750 | GGTGTGTGTGTGTTGGGGGT | - | 6.17 | RREB1 | MA0073.1 | chr1:228999728-228999748 | CCGGTGTGTGTGTGTTGGGG | - | 6.68 | Tcf12 | MA0521.1 | chr1:228999784-228999795 | CTGCAGCTGTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_49948 | chr1:228997517-229000847 | RPMI-8402 |
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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 |
GH01I228863 | chr1 | 228999708 | 229000807 |
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Enhancer Sequence | GACTGTATCC GGTGTGTGTG TGTTGGGGGT GGGGTGTGTC TAAGGTGATG CTGGGATTCT 60 TACACTGCAG CTGTTGTATC ACCAGCAGCA AGGATGATGG CGCAGGAGAC ACTCAAGGTC 120 ATTGCGAGGG GGCACAAACA CCTGGAGAAA GTAGCTCATC TTTGAGAGCA CCATGTGCTG 180 CAGTATCATT CAGTAGGACC TTTTTTTTTT TTCCGAGAGA GGATCTCTCT GTCACCCAGG 240 CTGGAACACA GTGGTACCAT CGTAGCTCAC TGCAGCCTCA AACCCCTGGG CTCAAGCATT 300 CCTGCTACTT CCAGCCTCCT AAGTAGCTAG GACTGTGTCA GCCAGGCTGT GCTTGAATAG 360 TGAGATTCAG GCATGGGCCA CAACACCCAG CTAATTTTTA AATTGTTTTG TAAAGATAGG 420 GCCTTGCTGT GTTGGCTTAG GCTCAATATA ACCTTTCTAT GGGACATTTA TTTGTTTAGT 480 AAACTTTCTC TGCCTCTCTC TCTCTGGTTT TGCTTTTAAC CCCAGAGGCC TAAGACTGAG 540 TTGCTGATCT TCCTGTTTTT GGCCCGATCA CACTCCTGAA AAGACTCTTT TAACTCTCAT 600 TTCCTGCTCC AGCCCCGTCC TCCCATAGGC AGCTTGCTGC AACCTGCTGT GGCTGATCCA 660 CTGGGTGGGC CCGAGCAATG GCTGCATTTC TAGTAGGGGG AGTTCTCCTT GCCACAGGAG 720 ATCACATACA CACTCCCTAG GCTGAGCTCA GGAATGCAAA CTCAAGTCAG CCTAACAGGG 780 TGAGGCTGTC CCATAGGAAG CAACATTTAG AAAAGAGTCA GGCCAGACTG GATTCCAACC 840 CTGCTGGGTG CAGATGGCTG GTCGGCAATG CCCCACAGCT GTCTTGGCCT TCCATGTGGA 900 CTGCTGAGGC TTCACATTTC CCCTTAGTAA CACAGCTGGG GCATTGCAAG GGGGTGGGGT 960 GGGGGAGCTG AACTGCAGAG 980
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