Tag | Content |
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EnhancerAtlas ID | HS050-00465 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:9526560-9527660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr1:9526701-9526712 | AATTTAATTAA | + | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27351 | chr1:9526007-9528246 | Esophagus | SE_30349 | chr1:9526146-9528836 | Fetal_Muscle |
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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 |
GH01I009466 | chr1 | 9526226 | 9528730 |
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Enhancer Sequence | GCACCCCTGT AATCCCAGCT ACTCAGGAGG CACAAGAATC ACTTGAATGC AGGAGGCACA 60 GTCTGTAGTG AGCCGAGATT ACATCGCTGT ACTCCAGCCT GGACAACAGA GCAAGACTCT 120 GTCTAAAACA AAAAAAAAAG CAATTTAATT AAAAAGCAGA GTTTTGTTGA ACTAAGATTT 180 CATCTCCTCT CTGGCCTGCT TGCTGGGCTA GACATGGAAG CTGCCAGCGC CATCATCTCT 240 GATTTTTTCG TGGTGGAAGA GGTGAGTTGT GCCGTCCTTC ACCACAGTGA CCTCCTGGGG 300 CCCAGCGCCT GACTCTGTGT CTGTGATGGA GGACACCTCA CATAGGATGG GCCCCAAGTC 360 CCAGCCGACA GCAGCACACA CACGCCTTGC TGCCAGATGG CAGCGCGAGC CTCTGTTTAT 420 GATTAGGTGG CAGACTACAC TCGGAACCCA GCAAGCCGAT GATGAAAGCT GTTAAAAGAA 480 CATTGTTATA TGACTTTTCA TAGTTTCCCA AGTAAATATT ACACTCACTG CTGCTTGAAT 540 TACTAATGCT TTGGAAGTGG AGGCCGAAAT CCATTCCCAA ACAGACTCCC TTTTTTTTCC 600 CTGTCACCTA GGCGCTCGGC ATTGTTGTCG AATTGTTTTC CCGGGCTCGC CCGTCCTCAC 660 AGCTCAGTAC ATTCCCTCCG AGTGATCTCT TGGCACCTCT GAAGCCCGAG TTTGCACAGC 720 CACCTCATTT CCCAGCTCCT CCACGCCAGC TCCCTCTGCA GCAGGCAGCT TGCCGCAGGC 780 AGGTGACCCA AAGGTCCTCA GATAGAACTG CAGAAAAGGG AGCAAATGAA AGGAAGGCAG 840 CCACGGCTCT GCCAAGCCTC TCCAAAGAGA CCCGGCTTTG CACAGGCAAC TTCAGGTGGA 900 AGGAAAGGAC CCTGCTGGAA ACGTCATCTC TGGGCCCGCA CTGCGGCATT TAACCTCTTC 960 CTTAGGCTGC CCGGAGAGAC AACTGGAGAA AGTGCCTTGG ACCCAAACAG CTCTTGGGTC 1020 CTCACTGTTT TTATTACTGC TTATAAAAGC TAGTAAACAG ATGGTTTGGG TTAGAGAAAA 1080 TATGCAGTCA GGGTTATTAA 1100
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