| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00163 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr1:12290180-12291710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr1:12291167-12291178 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr1:12291168-12291178 | TCAAGGTCAT | + | 6.02 | | RREB1 | MA0073.1 | chr1:12290962-12290982 | TGGGGGCGGGAGGGTTGTGG | - | 6.12 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGCCGAGC GGCTCCGTGC CGGGCGGGGC CAGGGTCGGG AACTGCAGGG CCGGCGCGGA 60
CCCGCGGGCC GCCGCTAGGG CTCCGCCTGG ACATGGGGGC CCGGGCCCAC CCTGGGGAGA 120
GCGATGCTAG GAGCCTGGGG GCCCCGTCGT CCGGCCTCGG TCTGAGCCCC TCGGGGTAAC 180
CCTGGGCGTC TGCTCCCCCC GGGCCCCAAG CCCGCCACCT CCGGGGACCC CTGCGTCCGA 240
GTCCCCGCGA GCTCCCCAAG CACAGGCTCG GGGCTGGCTG AACCTCTGGG AACCCCGACG 300
TCCGTGTCCT GGGGAGCCCG AGCCCCCGCT GGACCCCGGC ACACTTTCCG GGGTCCCAGC 360
AGCCTGGCGC CCTGGAATTG GGGGGTGTCA GTCCGCGCCT GTCCGCCTGA GCCTTGGTCT 420
CAATGCAGGA CCCCAGTGTG CGAGCCCCCC ACATTACGCC GAAGAGTGGG GTGTCAGTTC 480
TCTAGAATGC CTTAGCCACC TCCCTTAATC AGCCACCCGA GGTCACACTC TCGCGTGGAG 540
ACATCAGGCC TAAAACCTCT CTTTACCTTT TGCCCCCCAG GGTCACGCCC TGGCCCAGCC 600
ACTCCTCCTA GGTGTGGGAT GCCAGACATC AGGCCTAAAA CCTCTCTTTA CCTTTTACCC 660
CCCAGGGTCA CGCCCTGGCC CAGCCACTCC TCCTAGGTAT GGGATCCCGG CGCCGTTCCC 720
TCCAGGTTTT ACTTGGGTGG TGGGGTCTCT GTCCCCTGGA GGGGGCTGAG GGTTCCGAGA 780
GCTGGGGGCG GGAGGGTTGT GGGAGCGTCG CCTTCCGGGC AGTGCCGTTC CTGTGGGGCC 840
ACCGGTCGCA CAGCCGTCCC CGCCCCGGTT TTGGAGCTCC CTGGCGCCGG CAGCGTTCAG 900
CCCTGGCCGC CTCGGGGAGG GACGCCCAGG TCCGGTTGCC AGTCCTTCCT ATTCCCGGTC 960
TGGCCGCTCC TCAGGGGAGG GGCCTGGCTC AAGGTCATGC CCGGCTGTCT GCCCGCCCGT 1020
GGGCTCAGCA CTGATCCCTA CTGTCACCCG CCCCACTGGG TAGGGGAGCC CAGGTGGGGG 1080
TTAGTGCCAG TGCCAGGCAG CTGCCTAGAA GTCCTGATGG ACCGGAGTGT AAACACTTTG 1140
GGACTCTGGC CAGTCTGGCG GCCCTTGCTG ACACTGAATT CCTTCAGGGA ATCCTTGAAG 1200
TGGCCTCAAG CACGGTCTAG ATGCTTAGCA GAGCAAATAA TGGGTGCTTT CTGGTTTGGG 1260
CCTCAATGTT ACTGACCAGG TTGCCTCACA ATGCTAATCA CTCATGCTTT TAAAATCTGT 1320
GCTTTGCATT CTTTTCCGTT TAGGGCAAGT AGGGTAGGGC CTGAACTTGT TTACAAACTG 1380
ACAGTTGTTT CCCTTGATTT GGAGATAATT GGTAATTGGC ACTCAGAGTT GGCATTTAGG 1440
GCCGAAATTA GTGGCAATAA CTACAAAAAT AAAGAGTACT CTGACCTTGG CTTCTTGCTC 1500
AAATTTGTTT GGAGTCCCCA TAGTAAGATT 1530
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