Tag | Content |
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EnhancerAtlas ID | HS175-02375 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:185344380-185345770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:185345673-185345685 | CTCTGTTTACTT | - | 6.37 | FOXP2 | MA0593.1 | chr1:185345674-185345685 | TCTGTTTACTT | - | 6.32 | TCF3 | MA0522.2 | chr1:185345701-185345711 | AACACCTGCT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59999 | chr1:185306587-185355900 | Ly4 |
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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 |
GH01I185374 | chr1 | 185343791 | 185346891 |
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Enhancer Sequence | AGTAGATTAG TATGTCCAAC CCAGATTTTG GTAAACCCTA GACTCATTCT ACAGTCTGTG 60 ACATCTCCAT TTGGATTTCT TATTGGCATC TCAGACTCCA TATGTCTAAC CTGGAATGCC 120 TGATCTCCAT TGCCTCCTAA ACCGGCTTCT CTCACGGCTC TCCCATCTCG GGGCCCAGCA 180 TCTCAGACCT TTGCCTTGCT TACACCAGAC ATTTTGTTGT TATCTGTACC ACCTCCTTCT 240 CGTGCAGTCT ACTTGATGCC ACCTAATTGG TATCCCTGGC TTCTGCCCTT GTTCTCTTAA 300 CGAATCATTT TCCAAACAGC AGCCAGAGTG ATCCTTTCAA AAATGGATTC AGAAATCATG 360 TCACTGCTCT GCCCAAAGTT CCCAAATGAC TTCCCAGTCA CTCAGAGCAC AAGCTGACGC 420 TCGACACATC TGGGCCCCGT AAGATTTTCA TTTCTGCTCC TCCTCCTTTT GCTCACTCTG 480 CCCCTGCCAC ATTGGTCTCC TGCTTTCCCG GAACTTGCCC AACATGTTCC TCCCTCAGGG 540 CCTTCACATT TGTCATTTCC TGTCCTATGA TGCTCTTCCT GCAGATATCT ACAGCAGCTC 600 CCCGCTGCTC CTTTTGCAGG TTTTTGTTCA GATGTCATCT TCCTGGTGAG CTCTTCCCTG 660 AACAACTCCT CACCCCCTCC ACCTTGCCCC TGGGACTCCC TTTGACCTTT CTCGGATTGT 720 TTTCCCTGTA ACTCTTGCCA CCACCTCATA CAGGGCTTCT CAAGCTTGGC ATGATTGGCA 780 TTTTGGGACA GTTCTTTGTT GCGGGCTATT ATCCTGTGCC TTGCAGGATG TTTAGCAGCA 840 TCACCACCCT CGACCCACTC AATACCTGCA ACTTTCCTCC CTAGGTTGTG ACAGCCAGAA 900 ATGTCTCCAG ACACTGCCAA ATGTCTCCTG GGGGACAAAA CCACCCCTGG TTGAGAATCT 960 TTGATATAAT GTAAATATGC ATTTTACCTA TGTATTTGTT TATTGTTCCT CCCTTCCCCA 1020 CCAATAAAAT ATAATCTCCA TGAGAACAGG AATTTTTGTG TCTATTTTCC ACTGATGTAA 1080 TGCAGGCACT CTGAATAGGG TATGATGCAT AGTAGGTGCT CAAACAGATA TTTCACTGGT 1140 GAATAAATGA AATGTGCTCT GACCTTGTTC CTCTGTGCTC ATTAAGCTCT AGCCACACTG 1200 ACCTTTCTTC CACCTCTCAG ACATCTGAAG CTCCTTCTCA CCTTTCAGTC TTTTTCTTTC 1260 AGATCTCACT CCTGGAAAGC TCTATTCGCA GGTCTCTGTT TACTTGTTAC TCAGGTCCAA 1320 TAACACCTGC TTAGAGAGGC TTCCCTGATC ACCGTATCCT ACATGACCCT CCCTGCCAGC 1380 CAGAGTCACT 1390
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