Tag | Content |
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EnhancerAtlas ID | HS131-04297 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr19:934820-935660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZIC1 | MA0696.1 | chr19:935253-935267 | CGCGGCGGGGGGCC | - | 6.1 | Zfx | MA0146.2 | chr19:935107-935121 | CAGGCCTGGCCCGC | - | 6.24 | Zfx | MA0146.2 | chr19:935248-935262 | CAGGCCGCGGCGGG | - | 6.91 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_27633 | chr19:931683-935810 | Fetal_Intestine | SE_28572 | chr19:931612-935811 | Fetal_Intestine_Large | SE_47740 | chr19:934081-935683 | Pancreas | SE_57993 | chr19:932068-935605 | VACO_9m | SE_69171 | chr19:931842-935324 | H9 |
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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 |
GH19I000931 | chr19 | 931740 | 935806 |
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Enhancer Sequence | TGGTCTCAAA CTCCTGGGCT CAAGTGATCT GCCTCACTCA GCTTCCCAAA GTGCTGGGAT 60 TACAGGCCTG AGCCACGGTG CCCAGCCAGT CCTGGGATCT TATCCTGGGC TGTTCGTGGC 120 AGGTCCAGCC GCCGATGCCG CCGCCCGCCC AGCTGGCCAG ACACCTGTGT TCCCAGTGTC 180 AACAGTGGCC TGGGCCCAAC CAGCCCAGTC AGTGTTACCT CCCGCCCGGC CCCTACTGGG 240 GCCCCTGTTG ACTCTGGCGC CTGCCCCACC CCCTTCCTGG CACGTGGCAG GCCTGGCCCG 300 CTGGCCGGCC GCTTGGCACC GTCTCTGCCT CTTCCTCCCA GGTCCTGGCA GGGCTCGGGG 360 CTAACTTCCG CCTGCAAATC CTCGACAGCT GTGAAATTCT GCTGTCGGCT GCAGGTCTGG 420 TGGGTGGCCA GGCCGCGGCG GGGGGCCGGG CGCAGCAGGC TCAGGGCCAC GGGTTCTTTC 480 CTTGGACACC TGGAACCTTG CTGCCTGGGG CCTGGGGACG TGCAGTTTTG GAGGCCAGCA 540 CGTGTCGGGC AGTGATTAGG ATCTCAGCCT CCTGATGTCT GACGTAGCCT CCTGGTGGCC 600 TCCTGTCACC CACACAGCAG GCCCAGCTTC TAGAAAGCGG CCACGGTAGG ATTTTATTGG 660 ATTATTATTA TTTTTGAGGC AGGGTCTTAC TCTGTCGGGT AGGCTGGAGT GTAGTGGTGC 720 TGTCCTAACT CACTGCAGCC TCGATCTCCT GGGTTCAAGC GATCCTTCTG CCTCAGCCTC 780 CTGAGTAGCT GCGAGTACAG ACGGGCGCCA CCAAACTCAG CTAATTTTTG TAGAGACGGG 840
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