Tag | Content |
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EnhancerAtlas ID | HS007-17699 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr9:133298240-133299360 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr9:133298328-133298339 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr9:133298328-133298338 | AAAACAAAGG | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAGCACGTC TGACCATCTC TCAAAGCTGA GTGCAATCCA AAGTGGACTC AGATGCAGGC 60 AACTTCCTGT CCCCCTCACA ACCTCCCAAA AACAAAGGAA CTGCATTTAC AGTCAGACCA 120 AGAGTGTGTG AAACGGTCAG TGTTCTGGGG GTGCGGGCGC TCAGATTGTG GTTTCCCAAG 180 CCACCGATGG CTCCCTGAGG CTTTTCCCCA TTTAAGTTAA AGCTCAGGCT GATGGAAGTG 240 GAGGGATCTC CAGTCATGAG TGAGGGGTGC AGGCTGGAGG TGACGGGAAG CGGGAAACAT 300 GGAGAATTGA ATTGCCTAGA AAACCTAGAG GACTAAGAAG AGTCACCTGC ACACAGAGCT 360 CTCATGTACG GTGTCTGAGC GATGAATGCT CTGAGAGACT TGCAGAGCTT GTGACAGTGG 420 ACGTCACTGT CTCTCCCTTC CCAAGGAATC CCTGGCCCCT CGTGGGGGTC CAGGAGGGGC 480 AGTATTCATG GAGTCTTCAC TGAAAGTAGC TCCTCTGAAG CTGCCCTTGG CCATGGTCCC 540 GCATGAGCAG TGTGGGGTCA GGGGATTTTG CTGGGGAAGT CACTCTGAGC TGGCTGTCAG 600 CAGACAGCAG ATGAAGCGAG ACGCTGCCCA GACATGGCTG CTTATTCTAG CTGCAGGAGT 660 GTGAGGCCTG GAGAAGCATC TGGCCCCAAG CCCGTGGACC AGGCTTTGTT CCATGAAACA 720 GACGCACAGA GAGGCTGGGA AGGTGGTGCC CATGCACAGG GGCCTGGCCA GCTCCTGTGA 780 ACCTTGCAAA GCTGGCACCG TCCCTGACTC AGAGCAAGTG GGGAGCGGGT GTGTTCCCCT 840 TGCCCAGTCC ATGGCCCCAC CTGGTCCTGC GTGGAGGGCG GGGCATCACA TGAAGAAGAT 900 CTGAGAATCC ACGTCCAGGG CCATTTTTTG GTTCTTTTTT CAAACGGTTT GGAACAAACC 960 GGGGCTGGTC CAGAAGGGAT CTGCAAGTTA GAAAAGTTGG TTCACTTCAA CTCAGCAAAT 1020 ATATAATGAC AGTCTGTGGA GTCCCTGGCT CCGTGGTGAC CCGGGGCCCT CAATCGGTAT 1080 TTGTTGAACT GAGTTAAATA TCAACAAGGT ACATGCATTT 1120
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