Tag | Content |
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EnhancerAtlas ID | HS042-03063 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:173472580-173474240 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr1:173473641-173473652 | ATTGCATAATA | + | 6.02 | SP2 | MA0516.2 | chr1:173472697-173472714 | AAGTGGGCGGGGTAAAG | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCCCCCTCT CAAATGTCCC TGTTTTTCTT CCCTCAGAGG TTCGTAGTAG GCTCCCTAAA 60 GTCCAATACA AGGGCTGACA AACTCATATG AGAATAGGCA GATCACGTAA ACAGTTGAAG 120 TGGGCGGGGT AAAGGCGAGA GTGAGCAGTG TGGACTGTGG CAAGCTGCAG AGCATCTGCT 180 CCCTCTATAG AAGCCAAATG ATACTCAGCC CTATCTATTG CCACATACAG GAATGAGGGC 240 TGAGTGCTGG CAGACCTTAT TTTTTCATGA AAACTTCAAA ATCTGCATTT TTAAAATGCA 300 AAACATTTGT TTCTACTTGG CAACTAATTT TAAAATTTTA AAAGAAAACA AGTGACTCTT 360 AAACAAATTA AGAGTCAAAG ATCCAGTCCA CGTGCCTACC ATTTGTGACT TTTGTCTGAA 420 ACCCATGAGG AATACAAAGT GATGTGTTTC CCTCTATCTA AAAATGATTA CAGAGAAACT 480 CATCAAGAAA AGGGGCCTGT GGGCACAAGA ACACTAGGGA CCTGTGCCCT GCTCCCTGAC 540 AGTGCTTAAG ATCTCTGACT CAATAGCCCT TCTTAGGGTG CCCCAAGGGG GCTGACGCTA 600 GACCCTGAGT TCCCAGCCTT GCCATAGACT CCTGTGCCCC AAGAGTGATT TGAAAGCAGC 660 AGAGCGGCAG ACCTTCAGAG ACTGTGAGCT GGGGAAATGG TCATCTCAGT GCTAGCCAAC 720 TTGGAAAGGT GACCCAGGAG CAGAGGGGGC TCCCTAAATC ACAGTGCTGC ATATGACCCT 780 AGAAGAGGGT GAGCCACAGG AACCTCTGAG GTTCAAATTG CTGCCAAGGG AAAAGCTTAA 840 TTACTTATTG AATATCTGTC TCTCCTCCCT ATGAAGGCAA ACACCTTATC TGGCTCACTC 900 ACCAATTGGC ACTTGGCACA GTACCCAGCA CACAGCGGGG CTGCATTTTA TAAAAAGCAA 960 GCAATTGAGA AACAGTGAGA TATAAGACTG AGAAAACGTC ACTCTTCGCA CACAATTTGA 1020 AATCGTGCAA ATCCTCCCCC CAAAGCAACA ATCCATTAAG AATTGCATAA TAGCTAAACT 1080 GATGGATCAC ATGAATTGTA AACACTGGGA TGGTGCAAGT TAGAGTTACA AAGCTAGAGT 1140 GTGTCCTCAA GCTGGGGCAG CTGGGAGAAT TTTGTCATTG GGCTTGGGAG GGCAGGGATG 1200 CTGAGCACAA GATGGAAGAT CTTGTGTGTG TTTTTTCTAG AGCAAGCTCT TCCTATCAAG 1260 TCTTCTCTGT ATAATGCTTA GCACCATGAT GCATGCAGTT GGATGCTAAT AAATGTAACT 1320 ATAGCTACTC AGTGACTATC AAGGCATACT CAAGGCAAGT CATTTGACTT GTAGCTGTGA 1380 CCATGGAATA CTCACTGACT ATGGGTAAGG TTTCCTATTC CCTTCAGTTG CTGGGAGCAA 1440 ACCAGTTCCC CATACCTGGG CTCCTGTGAA AGAGTCTGTT CCCTCCCCAT TCTTGCACTG 1500 CCAGCACCAT GTGGCTGCAG CCTACCAGGG CAGCAACAGA GTGCATTGCA GAAGCTGCTC 1560 TCCCCTGACT AGTGTATGGA GGGAGGGACA TGGCAGAGGA AGGAGCCACC TGGATTTTAG 1620 GGTCTGGAAG TCTCTCATAT GTGACCTCCC AGGGCAATGT 1660
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