Tag | Content |
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EnhancerAtlas ID | HS146-02082 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr10:88739720-88740620 |
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 | GGGATTTCAC CATGTTGGTC AGGCTGGGAG GTTCCAATTT TATAAGATGA GAAGAAGGGC 60 TGAGGTCATG CCCATTCTGC CACTTTGCTG AGTCCAGAGC TATGATGAAG TGAAGAAGAA 120 GGCACAGGGC AGGACAAAGA AGGGAGCTCA GGGACCCGGG AGTTTTCCTT GGCAGAAGTC 180 AACTTGCCCC ACCCCTGAGA AAACTCTGAC CTTCTCAGCT GCCAGGGAGG AACGCAGGGA 240 CTGGGGAGGA GGGGACAGGG AGGGGAACAG TCTGCTGCTC TGTGCCCTGG GAGAGAAGTC 300 TGATGACGGC AGTAACTCAG GAAGGGTTAA GAATATTCCT AAAATAGCCA AGCCACAGTC 360 TAAGCCAGTC CATGAGCAGA GAGCAGATCT GTAGCAGGAA AAGTCAGCCT GATCTTTGCC 420 CCACTGCCTG CTGCCTAGCC CTGGCTGCTA ATTAAGCCTC CTACCCTGTC CCCTTCACCA 480 ATTCCTCTTG TCCTAGTGGG GATGGGGTAG GAGTAGTCAG AGGAGCCAAA TCACCCCAAT 540 CAACAGGGAA CTACAGCTGG GACCAGGAGC ACTGGGCCCA GTGGCCCCCC AATCCACACT 600 CCTGGTCTGA GAGTCAGGTA GGGGGACATA GGGAGAAAGA CAGGCAAAGT GCAGGCTTTG 660 TGCATGGGAT GGAGGCTGCC AAGAGAGAGC AGCCAAATTC TCCCACCCAC ACACATGCAT 720 CGCCAGCCAT GATCAGGTGG GACCTCCAAG ATCATCATCA GATACCGCCT TCTCCTAGCT 780 CTGTGTTCCC CTACACTTAG GGCATCTTGG AGTGAGACAG GCAGGGAGGG GTTGAGGGAG 840 CCCCTACATG AACAAACCAT ATCTTTGTTT CAGGGGCAGG ACCAGGTATA TAATTTGCAG 900
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