Tag | Content |
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EnhancerAtlas ID | HS104-24464 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr17:2951560-2952980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr17:2952845-2952856 | AGTAAACAGGA | - | 6.32 | MNX1 | MA0707.1 | chr17:2951842-2951852 | TTTAATTACC | - | 6.02 | Myod1 | MA0499.1 | chr17:2952592-2952605 | GGCAGCTGTCCCC | + | 6.29 |
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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 |
GH17I003048 | chr17 | 2951632 | 2953094 |
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Enhancer Sequence | TTTTCAAGTA TAAATCATTT CACCTGAAAT AATAATATTT TGTTTTCCTC CTGCCCCCCA 60 GTTTTAACCG CCTTGCCCCC TTTGAAGTCT TATATCTTGC CTGGGCGCTC CAAAACATTA 120 CATAAAAACG GTGAGAGCAG GGGCATTCGC ATCCAGCTCG ACTTTCATAG GAATGCGTCT 180 GGCGTTTCAA ACACTGTGAG GTTCACTATG GTTTTCTGAG TTGTCATTAA ATTCAGGTTT 240 GTTTAATTCC TGTTGACTAA AAATTTCATT TTCTTTTTTT TTTTTAATTA CCAATCAATG 300 TTACATTTTA TCAGCGCCTT TGGTCATCTA ACGGTCTGAT AGGCCATTGC CATTGCACAG 360 TGTTCTTCTA ACGGAATTTA GAATCCTAGC TTCCGATGCT TTCTCAGAAG AAGAGCACGG 420 GCGGTAGGAA AGAAGGACGC TTTCAGGAAG GATGGAGGGC CCAGGACGAT TTCGCTCCCC 480 GGTGGACGTG GAGGGCGGGC AGGGTCATCC TTTCTCCTGA AACTGGGGAG CCCTACGAAG 540 GGGTTCCGGA GAAGACGCAC GGATCTCGAA TACCTCCCCG CCCGGCTGCC ACTGGATGGC 600 GCGCGCAACC TGCGGAACCA CAGGGCGACA TCCAGCTGCG GGCGGCGAAG GGAATTGGAG 660 CGTGGACCTC TCCAGGCTTT TCATTCGCTG GTTCTGCCGG TGTCCCGCCT TTTCCATCTC 720 CTCATTGGCT GTCGCCTCCG GGCCTGCGAC TTTGCTCAGC CCCTCCGGGG AGTGGAATCG 780 GGTGTGCAAC AGGCCGTGAG GTCCGGCTTT GCGAGGAACT CCCATTGGTC AGTCAAACAG 840 GAGTCCCACC CTCCTGGGCT TCCCATTGGT TGCTGTCCCA CCGCTGCTCT CAGTTTCCCA 900 GCGGCTGGGG ATCTGGGTTT TCTGGGGGTG GAGGGGTGCA GTACGCTGCT GGAAGCTCGT 960 TTCTCTTTCC ACCGTTGTGT GCCTCGGGCT CGCGGTCAAC GGGGCTGGAC GAGGTTCAGA 1020 ACCCTCCAGA GCGGCAGCTG TCCCCGGGGT GGGTTGTGGG ACTCAACAGC CCTCAGGGGA 1080 AAATGGCGGG AGGCAGGTGG AGGTGTCTTC TTTGCACTGA AGACCTGGAT ACCCTGCTGC 1140 GGGCTGAACG GGAGGCTGGG GTGGAGCCCT GGCTCGGGTT ATGGCCGGGG AGGAGACCAC 1200 GCTGGGCGAG TGGGAGGCAG CCCCAGCCAG GGGCTGGAAG ACCAAGTACC GGACCTTCAA 1260 GGGCCTTCTT GCACCCGCAT CCCACAGTAA ACAGGATACG TAGGTGACCG TCTAGAAAAC 1320 TTGAGTTTCT CTTGACAAGT TGATGTGCCA GTTTTCGTAT GCATTCAAAT AAATATTTAG 1380 TAATTTCAAC TTTGCGCTTT TAGCATTTTG GAGCTAGTAA 1420
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