Tag | Content |
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EnhancerAtlas ID | HS101-05652 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:88739660-88740590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr10:88740307-88740318 | CCCAATCCACA | + | 6.14 | ZNF263 | MA0528.1 | chr10:88739964-88739985 | GGAGGAGGGGACAGGGAGGGG | + | 6.51 |
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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 |
GH10I086979 | chr10 | 88739157 | 88740602 |
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Enhancer Sequence | AGCTGGGATT ACAGGCACAC ACCACCATGC CAGGCTAATT TTTGTATTTT TAGTAGAGAT 60 GGGATTTCAC CATGTTGGTC AGGCTGGGAG GTTCCAATTT TATAAGATGA GAAGAAGGGC 120 TGAGGTCATG CCCATTCTGC CACTTTGCTG AGTCCAGAGC TATGATGAAG TGAAGAAGAA 180 GGCACAGGGC AGGACAAAGA AGGGAGCTCA GGGACCCGGG AGTTTTCCTT GGCAGAAGTC 240 AACTTGCCCC ACCCCTGAGA AAACTCTGAC CTTCTCAGCT GCCAGGGAGG AACGCAGGGA 300 CTGGGGAGGA GGGGACAGGG AGGGGAACAG TCTGCTGCTC TGTGCCCTGG GAGAGAAGTC 360 TGATGACGGC AGTAACTCAG GAAGGGTTAA GAATATTCCT AAAATAGCCA AGCCACAGTC 420 TAAGCCAGTC CATGAGCAGA GAGCAGATCT GTAGCAGGAA AAGTCAGCCT GATCTTTGCC 480 CCACTGCCTG CTGCCTAGCC CTGGCTGCTA ATTAAGCCTC CTACCCTGTC CCCTTCACCA 540 ATTCCTCTTG TCCTAGTGGG GATGGGGTAG GAGTAGTCAG AGGAGCCAAA TCACCCCAAT 600 CAACAGGGAA CTACAGCTGG GACCAGGAGC ACTGGGCCCA GTGGCCCCCC AATCCACACT 660 CCTGGTCTGA GAGTCAGGTA GGGGGACATA GGGAGAAAGA CAGGCAAAGT GCAGGCTTTG 720 TGCATGGGAT GGAGGCTGCC AAGAGAGAGC AGCCAAATTC TCCCACCCAC ACACATGCAT 780 CGCCAGCCAT GATCAGGTGG GACCTCCAAG ATCATCATCA GATACCGCCT TCTCCTAGCT 840 CTGTGTTCCC CTACACTTAG GGCATCTTGG AGTGAGACAG GCAGGGAGGG GTTGAGGGAG 900 CCCCTACATG AACAAACCAT ATCTTTGTTT 930
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