Tag | Content |
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EnhancerAtlas ID | HS047-15669 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr18:9625120-9626270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr18:9625782-9625793 | AGTGACTCATG | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64254 | chr18:9625478-9626693 | NHEK |
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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 |
GH18I009625 | chr18 | 9625284 | 9626471 |
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Enhancer Sequence | GGAGGCGGAG GTTGCAGTGA GCCGAGATTG CACCACTGCA CTCCAGCCTG AGTGACAGAG 60 CGAGACTCCA TCTAAAAAAC AAAAAAAGAA AATGATAGGC TACATCAAGA CCACAGATTA 120 GAAAGCTCAA TTTTATGAAA GGTCAATTGT CTTTCAAACT GATTTATAGA TTCAATTCAT 180 TCCTGATTAA AATCTGAGCC AATTTTGTTG TTGTCGTTAT TGTTGTTGTT GTTTTGAGAT 240 GGAGTCTTGC TCTGTCTCCT AGGCTGGAAT GCAGTGGTGC GATCTTGGCT CACTGCAACC 300 CCCGCCTCCC AGCTTCAAGC AATTCTCCTA CCTCAGCCTC CCGAGTAGCT GGGATTATAG 360 GCTTGTGCCA CCATACCCAT CTAATATTTG TACTTTTAGT AGAGACGGGG TTTCACAATG 420 TTGGCCAGGC TGGTCTTGAA CTCCTGATCT CAGGTGATCC ACCACCTTGG CCTCCCAAAG 480 TGCTGGGATT ACAGGTGTGA GCCACTGTGC CCGGCCTAGA TTTTTTTTAT GGGTGGCCAG 540 AAGTCTGACA CGGATCTCAC TGAGTTAAAG TCAGGGTGTC AGCAGGGCTG CATTCCTTTC 600 TGGAAGCCCT AGGGTAGAAT GCATTTCCTC TCCTTTTCCA GCTTCTAGAT ACCTCAACTT 660 TCAGTGACTC ATGGCCTCCT TTCTTCATCT TCAGCAACAT TGCATCTCTC TGACCCTTTC 720 TCCAAAGTCA TGTCACCCTC TGTCTCTTTT TCTTTCTTCC ACTTTTAAGG ACTTTATTTA 780 TTTATTTATT TATTTATGAG ACAGAGTCTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGGC 840 ACAATCACTG CAACCTCTGC CTTCTGGGTT CAAGTGATTC TCCTGCCTCA GCCTCTCAAG 900 TAGCTGGAAT TACAGGCGCA TGCCACCACA CCCGGCTAAT TTTTATTTTT GTATTTTCAG 960 CAGAGATGGG ATTTCACCAT GTTGGCCAGG CTGGTCTCAA ACTCCTGACC TCAAGTGATC 1020 CATCTGCCTT GGCCTCCCAG AGTGTTGGGA TTACAGGCGT GAGCCACTGC GCCTGGCACT 1080 TTTAAGGACT TTATGATGAC ATAAAGTTGA TAGTGGATAT TGACTACCTG ATTCTAAAGG 1140 TATATGCAGA 1150
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