| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00268 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr1:12290320-12291780 | 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 | GCCCCGTCGT CCGGCCTCGG TCTGAGCCCC TCGGGGTAAC CCTGGGCGTC TGCTCCCCCC 60
GGGCCCCAAG CCCGCCACCT CCGGGGACCC CTGCGTCCGA GTCCCCGCGA GCTCCCCAAG 120
CACAGGCTCG GGGCTGGCTG AACCTCTGGG AACCCCGACG TCCGTGTCCT GGGGAGCCCG 180
AGCCCCCGCT GGACCCCGGC ACACTTTCCG GGGTCCCAGC AGCCTGGCGC CCTGGAATTG 240
GGGGGTGTCA GTCCGCGCCT GTCCGCCTGA GCCTTGGTCT CAATGCAGGA CCCCAGTGTG 300
CGAGCCCCCC ACATTACGCC GAAGAGTGGG GTGTCAGTTC TCTAGAATGC CTTAGCCACC 360
TCCCTTAATC AGCCACCCGA GGTCACACTC TCGCGTGGAG ACATCAGGCC TAAAACCTCT 420
CTTTACCTTT TGCCCCCCAG GGTCACGCCC TGGCCCAGCC ACTCCTCCTA GGTGTGGGAT 480
GCCAGACATC AGGCCTAAAA CCTCTCTTTA CCTTTTACCC CCCAGGGTCA CGCCCTGGCC 540
CAGCCACTCC TCCTAGGTAT GGGATCCCGG CGCCGTTCCC TCCAGGTTTT ACTTGGGTGG 600
TGGGGTCTCT GTCCCCTGGA GGGGGCTGAG GGTTCCGAGA GCTGGGGGCG GGAGGGTTGT 660
GGGAGCGTCG CCTTCCGGGC AGTGCCGTTC CTGTGGGGCC ACCGGTCGCA CAGCCGTCCC 720
CGCCCCGGTT TTGGAGCTCC CTGGCGCCGG CAGCGTTCAG CCCTGGCCGC CTCGGGGAGG 780
GACGCCCAGG TCCGGTTGCC AGTCCTTCCT ATTCCCGGTC TGGCCGCTCC TCAGGGGAGG 840
GGCCTGGCTC AAGGTCATGC CCGGCTGTCT GCCCGCCCGT GGGCTCAGCA CTGATCCCTA 900
CTGTCACCCG CCCCACTGGG TAGGGGAGCC CAGGTGGGGG TTAGTGCCAG TGCCAGGCAG 960
CTGCCTAGAA GTCCTGATGG ACCGGAGTGT AAACACTTTG GGACTCTGGC CAGTCTGGCG 1020
GCCCTTGCTG ACACTGAATT CCTTCAGGGA ATCCTTGAAG TGGCCTCAAG CACGGTCTAG 1080
ATGCTTAGCA GAGCAAATAA TGGGTGCTTT CTGGTTTGGG CCTCAATGTT ACTGACCAGG 1140
TTGCCTCACA ATGCTAATCA CTCATGCTTT TAAAATCTGT GCTTTGCATT CTTTTCCGTT 1200
TAGGGCAAGT AGGGTAGGGC CTGAACTTGT TTACAAACTG ACAGTTGTTT CCCTTGATTT 1260
GGAGATAATT GGTAATTGGC ACTCAGAGTT GGCATTTAGG GCCGAAATTA GTGGCAATAA 1320
CTACAAAAAT AAAGAGTACT CTGACCTTGG CTTCTTGCTC AAATTTGTTT GGAGTCCCCA 1380
TAGTAAGATT AGTCAGTTTC ACATTTGGTT TTCACAAATT TACTCCTTTC AAGTTATAAT 1440
AGTGGCCGGG CACGGTGGCT 1460
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