Tag | Content |
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EnhancerAtlas ID | HS104-05821 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:227079560-227080530 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr1:227079753-227079765 | GGCCACGTGCCC | + | 7.22 | ZNF263 | MA0528.1 | chr1:227079627-227079648 | GGAGGAGGGCATGAGGGGAGG | + | 6.49 |
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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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Enhancer Sequence | TCACACGGCC TGCTTCAGCC TACGGCGGGA GCGGAGACAG AGGGTGGAGG CTCCCTGCAG 60 CCTGGGTGGA GGAGGGCATG AGGGGAGGGG CCCCTTTTCC CATCAGAGGC ATCTCTGTGA 120 AAGTAGAAGA TGCCTGCAGC GCTGGGGTCT TCTCAGCAGG CCCCATGTAG TTGTCCGGCA 180 TGTATTGAGT ATGGGCCACG TGCCCGTGCT GTGCTGGGTG AGGCCCAGCC CTGGTGGGAC 240 CCACAGGCTA AGGAGACACG GGCAGTAATC ACATAGACTG AGAAGCCAAG GACTATGAAG 300 GGGGCCATGG GGTTGGGGAG GGGCGGCAGG AGAGCATGCC ACGGGGCTTC TTGACCTGGT 360 TGGCAGGGGT GAGAGAAAGT CAGCTGAGGA AGTAACTGCT GAGCTGAGCT CTGAAGGTTG 420 AGTCACAGCA GTCACTAGAG GAGAGGAGCA CAGGGTGGGG AGCATTTCCT GACAGACAGA 480 CTCAGGAATC AGAGGAAGCC GGGGCGGGAT GCAGAGAGCA GAAGTGTGGG AGAGCCTTGC 540 AAACAGGCCT GGAGACATGC GAAGATAGGA GTTCATCCTG GCGTCAGTAC ACGGTGCCTG 600 CCTAACACCC AATGCCAGCC CACTGCTGCG TGCCAGGCAG CACCCTGGAG CAGGGAGATG 660 CTGCACTGTC GTAACAGCCC CTGCCTTGAG AGGTGCCTTA CGGGAGCAGC CTGGTGACAG 720 TGGCTTGGCA TACAGGACTC CAGTGACACG GGAGGGGCAA GCTAGGGAAA GATCACTCTG 780 CGGTGGGTCT GGAAGGAGGA GCAGGTGCGC ACCCTCCAGG CAGGCTTGGG GGAGGTATTT 840 ATTCCAAGGC CAACTGGTGT GCTGCAGACC AGGAGTTAGC ACAGATCCCA CGGGGCCCGC 900 AGGACTGGCC TCCCTCCAGA CACCAGCCAC AAGCTCTAGA GGGTCTAGAT GCCACTTGTG 960 CTTCTGACCG 970
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