| Tag | Content |
|---|
EnhancerAtlas ID | HS017-34790 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chrX:101914380-101915850 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chrX:101914564-101914576 | GAATGTTTGTTT | + | 7.22 | | GCM1 | MA0646.1 | chrX:101915247-101915258 | GATGCGGGTAC | + | 6.14 | | MITF | MA0620.2 | chrX:101914857-101914875 | GTGGGTCATGTGACCAGG | + | 6.09 | | MITF | MA0620.2 | chrX:101914857-101914875 | GTGGGTCATGTGACCAGG | - | 6.09 | | Myod1 | MA0499.1 | chrX:101915173-101915186 | AGCAGCTGTTGCT | + | 6.59 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCCCACCT GATCTTATTT CTCATTACTT CCTATTTCTG GTTCATTATA AATGATATAA 60
ATTAAATTCC AATATGATGT TAGTTTGCTA AGGTTTACGA AAGCAGGGCA AAGTGGCAGT 120
TTTGCCTCCC TTCACAAATC AAAAATTTTA ACAGGGATCA TCCTGGTGGT GCAAATTGGA 180
GTTTGAATGT TTGTTTTGCT TACCAGCATT TTTCAAGACA GATCTTGCGT GTGTTTTAGT 240
ATGTCGCTCT AGTCGTATAC AAAATATCAC AAATCACTTC ATCTCCCCAA TCCTCATCGA 300
ATGTTCCTCG CCAGCCCAGT GGTCCTCCAG AGCAAAGCCC GGCCTTCCTT CCAGCTGTCT 360
GGGCCAGGAG CTTGAGGGTC TTCTAGCAAG CACCCCGGAG GCTGTCTTCT GACTGTCATG 420
CAGGGCTGTG GCAAACTAGC TGACTGCGCA GTCACGTGGA GGGGGGAGGG GCTGACGGTG 480
GGTCATGTGA CCAGGCTCTG GGTTGAGCCG GCCTAGAGGA GTGTTTTCTT ACACCCAGAA 540
AGTACAGGAA AGGCAGACGA CAACTGTGCT CCGCAGAGCG GGAGGTGGGG GGAACGGCGG 600
AATATTAAGG TGGGTAGGTG TCTCTCCATG CTTCATCAGC CTGAAAACTA ATTTCTCAGG 660
CGACCGGAAT TACAGCATTT CTTGGTAGAG GAAACTATCC CTCAGCCAAC CGCTAGCGGT 720
CTTAGACGGT CTGTCTTTTG TCCAGGAGCT CAAGAAGCAG AGACTCTACC TGCCCTAGGC 780
GTTCGTGAAG AGAAGCAGCT GTTGCTATTG GAGGAGGTGG GTGCAAGGAC GGCAGATGCC 840
ATCCCTGAGA GGCGGTGACT GAGACTAGAT GCGGGTACAG GTAGTGCCTC GGATCCCCGG 900
GCTGCCTCCT GCCTTTTGAA CATCCCAGGG GTCCCAACCC AGCGCCCTGT GTTTCTATGT 960
GTGGGTGGGA GAGGTGGGCA TATGGATGGA GTTGGCTTCA GGGGAGCCCA GAGAGGGGAA 1020
ATGGTGAAGT GACAATTCGT GAACACGTGT GGTGCTGGAT CAGGAAAGGT AAGGGTGGGG 1080
ATGGGAACCA TGGACTATGC TACTGCTGTC TTCCTCCCAC CAAGTAGGCA CTCACTCTGC 1140
TCTCTGTCTG TCTGTTTACT GGCAGTATTC AGGCAGTGGG GATGGCTGAT ACCAGCTCAA 1200
AACTGGCGGA GGGTGGAGGA GGGCAGAAGA GAACACATAC ATCTGCCTTT TGCTCCAAGG 1260
CTCCAGCTGG CTGGGGATGC AAGAGAGGAA TGAACCTCAA TCCAGGCAGT TCTAGGAAAA 1320
GAAGGAGGAG ACATAGACTC GAGGGGAGGA AACCTAGATG CTGTGGGCCC TTCACTTAGG 1380
ATTTCTCATT AGGATACTCC AAGCTTCTCG ACCCCCAAGG GGATTCCTGG ATCTCAGCCC 1440
CATGCAGCAG GATCTCATTC CCATTGAGGG 1470
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