Tag | Content |
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EnhancerAtlas ID | HS042-31314 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr3:14824940-14826310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr3:14824981-14824992 | TAATTTAATCA | + | 6.62 | RREB1 | MA0073.1 | chr3:14825311-14825331 | CCCCAACACCCCCACCCAGA | + | 6.36 | RREB1 | MA0073.1 | chr3:14825309-14825329 | ACCCCCAACACCCCCACCCA | + | 7.85 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53487 | chr3:14824865-14828081 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 14825074 | 14825174 | chr3 | 14825602 | 14826242 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I014783 | chr3 | 14824866 | 14828081 |
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Enhancer Sequence | AAGGATGTAA GAGCAAAAGA TAAAATTGTC AGTATTGAAG ATAATTTAAT CATCTACCTA 60 GAAAAACCAA CAGAGTCAAT AGACAAACTG TTAGAACTGA CATAGATTCA GCAAGATGCC 120 AGATGCAAGT GCAACCTATA AAGCTGGTTT CTCATAGTGA AAAGCAGCAG GCCAGGCTGC 180 AGGCACAGCA ACACAAGGTC TCAAAACACA CAGATGATGG ATAAAAAACA GTGGCATTAG 240 GTGCCAGGAA TGGACTGAGG CAGGAAAAAG ACAGTGTGCC TGAGAGGATG GGGCCCCTCT 300 GCAGAGGGCC TGGGATGTCC TCCTAGGCCA CAAAGATCCA GAATAGATAC GTGGCTGCAG 360 GTTGCTGAAA CCCCCAACAC CCCCACCCAG AACCCTCAAA TATTTACCCC TTCAATAAAT 420 ATTAACAACA CCTCTTTCTC CCTGCACTGC CCCCCACTCT GGCCTTGAGG CTATGGGCAA 480 GCAACTTTGG TCTCTGGACT GCCACTTCCT TATCTATAAA ATGGGATGAT CCCAATAAGC 540 AACTTCCCAG GGATATTGGG TGGGTTAAAT ATGATAATAC AGAGAAAGGA TTTAGCTCAT 600 GCTTACTAAA CATAAGTGAG AATAACTATT AATAAAATGA TTAAGGCGCT CCCCCTGCCT 660 TCCGTAATGC CAGCCTGCAC TCCAGCAGGG CCCACCCCAC TGCGGGCTGC TTCCAGTCTG 720 CAGCTCCCTC AAGGGTTAAG TGGCTTGGCT GCGGGCCAAG GAGCAGGAGC AGGAGCAGGA 780 ATAAAGCATC AGCCCCAGCA GCAGCATCTC CCTATCTGTG AGCAATCTCC TCTGGCCCCC 840 AGCTCAGGCC TTGGGAAATA AAAGCCCAGC CAGCTCCTGC CAGCTGCATC ATAATGACTT 900 TCCCCTTCCA GGAAGGAGAT TGGGTGGGCC TTCCCCTCCT GCCTCTTTCT CCCTTCCCTA 960 GGTTTAGGGG CTGCTGGGGA CACGTGAACT GCCCCGAAGC TGTCAGCTCA CATATGAGAA 1020 AGAGAGTGGG TTGTTTCGGC TGCTGGCCCT GTGGGGTTGG AGGGAAGGAC AACAGGGAGG 1080 GGTCCTGGCT CTGGGAGGTG GGGAGCAGGA GGTAGGAGGT GCCCAGTTGG TATGCCCTTG 1140 GTATTCTGCA TCTCAGCGTA TCCTCCCCTG GGTCTGGACA GGATGTTTCC AACTGCAGCT 1200 TGTGACCCAG TAGTGAATTG CAAAATCCAT GGAGTGGGTT GTGATGCGCA TTTTGAAAGA 1260 GACAGCTGGG ATAGAAAATA CGCCTTGCAT ATAATAAAGC ACAGGCTTTA TTTCAGTCAC 1320 CCATGAGTAT AGTGGTTAAA AATGCAAGCC CCAGGCCAGG TGCGGTGGCT 1370
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