Tag | Content |
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EnhancerAtlas ID | HS006-33242 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr5:138897100-138898400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr5:138898206-138898218 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr5:138898210-138898222 | GTTTGTTTGTTT | + | 6.32 | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 138897527 | 138897822 | chr5 | 138897122 | 138897400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I139517 | chr5 | 138896810 | 138898710 |
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Enhancer Sequence | CCTGGGCGAC AGAGCGAGAC TCCGTCTCAA AAAAATAAAT AAATAAATAA ATAAAATAAA 60 TAAATAAATT TCCTTCCTCC AGCTGCAGGG CAAAAAATGG GTTGAAGAGC CGGACTGGTG 120 GTAACTGGTG TGGCCATCCA GCCTGGAGTC GATGTTGGCA TGAATGAAGA CACAGGCAGT 180 TGGGACAGAG AGAAGCGAGT GGGATGTGGA GGTGACCCGA TGAAATACTG GCCCGGAGAT 240 ATGAGGCATG AGGCGGGGAG CACGAGGGTG TCGAAGGGCC AAAATGTGGT AAGAGAAGCC 300 GGAGGAGTGT GAGGACAGGT GGAAGGGATC CAATGTGGGA TCTAAGGGGT CTGAGACCAC 360 CGTGGCCGCG GGAGGCAGGA GAAGGTACCG CAGAGCTCCC GGTGATGTGT CAGGAGGCCC 420 TACACTCGCG CGTGCACTGG CTCGCAGTTT GGACAGAGAC CCTACAGGCC AGGCCGCAGC 480 TGCGCCCAGA CCACCCCCAG CGGGTGAAGA CTGCCGCGGC GGCGCAGTTC CCGGCATGCC 540 TCCGGCCGGT GACTTCATCC GGCCCGGGGC CAAGGCCCGG CCTCCGCTAG AGGGCGCTGC 600 TCTCAGCAGC CGCGCCGCCC GGATGGACTC GCGCCAGAGT AGGACAAGAG AGGCAGGCGG 660 CGGCTGCTCC GTGCGGCTCC CACGCCTCTC GGGCGGCAGG TCCTGCCTCG GACCTGGGAC 720 CACTGGCTGG CGCCTGTGGC TCACATCTCC ACGCCTTTGC CCGCTCCTCC CAGGAGCCCG 780 AGTCAGAAAC CTGTGCTTCA CCCTCGAGAG CGCTGCCATC CTCCCCCTCA ACCAGACGGG 840 CATGGCGTCT GGTTGTCCGT CCTGTCTTCT CATCGTCTCA GAGCCCTTCC CTGACCCCTA 900 CCCTCTCTCA GACCAACAGG ATGATGACAG GAAGAGGATC CAGGACCAAC TCCTAGCGGT 960 GACCTTGAGA AAACAATCTC ATACCCCAGT TTCCCTTACA ATGCAATGGA AATAATACTA 1020 ACAACCCTGG AAGAGTGTTG GAAGGACTAA ACGAAATCAT CTTTTTCAGT ACTAAGCAGA 1080 GGCTCAGTGA GCATCAGCGT TTTTTTGTTT GTTTGTTTGT TTTCTTGAAA CTGGTTGGAG 1140 CCCAGGCTGG AGTGCAGTGG CATGATCTTG GCCCACTTGA GCCTCAATTG CCTGGGCTCA 1200 AGCCATTCTT CCTCCTCAGC CTCTGGAGTA GCTGGGACCA CAGTTGCATG CCACCACGAC 1260 TGGCTACTTT TGTTCATTTT TTTTGTAGAG TTGGGGTCTC 1300
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