Tag | Content |
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EnhancerAtlas ID | HS141-01359 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:168438620-168439800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:168439109-168439120 | CATGAGTCACT | - | 6.14 | MYB | MA0100.3 | chr1:168439663-168439673 | ACCAACTGTC | + | 6.02 |
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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 |
GH01I168465 | chr1 | 168435001 | 168441170 |
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Enhancer Sequence | ACTAGAGAAA AGAGTATTTC CATTTTCCTC TGTAAAACCA AGTTGGCCCA AACGTATATT 60 CCTCCTTTTA TATGATTAGT GTGAGCGTTC AAGCTGGGTG GAGGCAGGGC ATCTCTTTTG 120 TAATAAGTTG TCACCAGAAA GTCTCATTTT GTTGAGAAGA GAAACCCCTG CAATTGATGG 180 GACTTGGAAC AAACTTTCTG GGACACTAAA TGGCAGGAGA GCCAGTGTTT TAAGAAGTCA 240 TTTCTGTCCT GGTTTGTTAT TAAACTGTGG AGCTTCCTTT TCAAGATAGT AAAGATAGTA 300 ATAAGTCATG TAATACAAAT TGATTCAAAA GGAGACTTAG GGGCTTACAG AATCCCAAGA 360 CAGACAAGCA TTAAAAGTGC CTGCGGATCC GGCAGGAAGC CAATCCCCAG ATGTTACTTT 420 TGGCTGGGAA GGGTGAGGAG GAAGCGGTGG CCTTGCTCTG GCTTAATCTG CAGTGACAAC 480 CGTGGCGAGC ATGAGTCACT CTGGGCCTCA TCTGAACCCT ATCTTGGCAT CTTGCTTGTG 540 GAGAGGCAGT GCTGTATAAT GGTTCAGAGC AGGCTTTGGA ACAGACTGCC TGGACAAGCT 600 ACTTAATTGC TCTGTTCCTT AGTTTCCTCA TCTGCAAAGT AGGGGGAAAT AGCAGCACCT 660 ACCTCGCTGG GTTGTTGTGA AGTTTAAATA AATTAATACA TGTGAAGTAC TTAGAACATT 720 GCCTGGCACA TTTGCTAGAT GGTCAATAAA TGTTGCATAT TATTTTATAT GGGCTATTTC 780 TTCAGTTCAG TATTCTGAGT CTCTAATCTG AGAAACTTGG TGGCACAAAT ATTTCCTAGT 840 TAGGCAAGCA CTTTGTAATG TTTTTAATTT GTAATAGAAA ACAAGGATAA CTTAGCAAAT 900 GAATACCCAC AAGCAAACAC TGCACTTCAT TTTAACCAGA CAATCCAATA TCTTTCCCTA 960 GCACACTTTT GTTCTGAGAG GGAAATCAAA GAAACTAGAG CTTTCTTTCT TTCTCTTAAT 1020 CCTGCATACC TTCCACTGTA GGTACCAACT GTCATTTAAT AAAAGCTCTG CAGCAGAAGA 1080 GAAAACAGGC AGAGCAAACA GCCCTAATAA TTTACTTATT TTTGATTCAC ATCCTAATAA 1140 TAATGGTCAC CATGGTTTAG AGTAATATTG AATTCCTATT 1180
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