Tag | Content |
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EnhancerAtlas ID | HS098-18476 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:100488860-100489760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA | MA0729.1 | chr14:100489517-100489535 | ACTTGTCCTTTTGCCCTT | - | 6.58 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_43398 | chr14:100488769-100489643 | MCF-7 | SE_46576 | chr14:100488509-100492126 | Osteoblasts | SE_52148 | chr14:100488767-100489446 | Skeletal_Muscle_Myoblast | SE_63969 | chr14:100488797-100489687 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I100022 | chr14 | 100488846 | 100492929 |
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Enhancer Sequence | CCCACCTTGG CCCCCAGAAG TGCTGGGTTT ACAGGCGTGA GCCACCACAC CTGGCTGGCC 60 ACATTCGTTT TTAAAAGGAA GTCTGATTTT GACTCAGATG CATTTACTTA TTGGACTATG 120 AATTCCATGA GAGCAGAATT CATAAAAACA ACAGAATCCT GCCTGTTTTT GTTTCCTTGG 180 CACCTACAAC TGCTTGACAC ACAGTAAGAC CTTAATGAGC AGTTGGTACA GTGCATTTTA 240 ACCAGAACTT AAGGAAAAGC AAGCAAGCTA TCCAGCTAGC TCGGCACAGT CCTGAGGTCG 300 GTGCCATGGT GCCACGTGGG CTGTTTTGTG TGCTGGTTCA GGAGAACGTG TGGAAAAGCT 360 GATAACTGAT CTCCTGAGAA AAGCGTGGTG TCCTCAGCAC ACCCCACTTG CTGGAGTGCC 420 AGAGAAGTCA TCACGTTTCA TTAAGGAATC CCTGCAGATG ATCTCACTCC ACTGAGCACT 480 GATGGTTGTG ATGATTTACT GCTGCCTGGG TCCCACGCCT AGAGAGTAAT AGGAGCTTGA 540 GAGGTTGGGC CAGTGTTTTA CAGCTGCCTA GGGGATTTTT GTCTGCCATT GCCTACAAGA 600 CTATTGTTCT ACCACCAGGC AAGCTGTTCT AGCTGGCTCT TGGGGTAGAC ACAGGTCACT 660 TGTCCTTTTG CCCTTTTTTT TTTTTAATTT TTTTTTTTTG GAACACAGTC TCACTTTGTC 720 ACCTGGGTTG GCGTGCAGCG GCAGGATCTC AGCTCACTGC AACCTCCACA TCCCAAGTTC 780 AAGCAATTCT CCTGCCCTAG CCTCCTGAGC AGCTGGGATT ACAAGTGCCC ACCACCAAGC 840 CCGGCTAATT TTTTTTTTTT TTTTTTTTTT TTTGAGATGG AGTTTCGCTC TTGTCTCGGG 900
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