Tag | Content |
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EnhancerAtlas ID | HS098-27058 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:9896000-9897060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP1 | MA0079.4 | chr19:9896387-9896402 | CAGACCCCGCCCCCA | + | 6.25 | SP4 | MA0685.1 | chr19:9896387-9896404 | CAGACCCCGCCCCCATC | + | 6.43 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28527 | chr19:9894046-9897642 | Fetal_Intestine |
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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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Enhancer Sequence | GTAGCTGGGA CTACAGGCGC CTGCCAGCAT GCCCAGCTAA TTTTTGTATT TTTAGTAGAG 60 ATGGGGTTTC ACCATGTTGG CCAGTATGGT CTTAATCGAT TGCCCTCGTG ATCCGCCTGC 120 GTCAGCCTCC CAGTCTGTCC CCTCACCACT ACTCTCTTTC ACGGAGACCC CACCCCCATC 180 TCTCCCTTCA CCGACTCCCC GCCCCCGTCT CTCGCTCACG GAGTCCCCGC CCCTGTCTCA 240 ACCAAGACCG AGTCCCCGCC CCCATCTCTC CCTCGCCGAG TCGCCGCCCG CGTCTCTCCC 300 TCACCCAGAC CCCGCCCCAT CTCTCCCTCA CCGAGACCCC GCCCCATCTC CCCCTCACCG 360 AGACTCCGCC CCCGTCTCTC CCTCACCCAG ACCCCGCCCC CATCTCCCTC TCACCGAGTC 420 CCCGCCCCCA TCTCTCCCTC ACCAAGACCT TGCCCCCATC TCCCCCTCAC CGAGGCTCCG 480 CCCCCGTCTC ACCCTCACCG AGACCCCACC CCCATCTCGC CCTTCACCCA GTCCCCGCTC 540 CCATCTCTCC CTCACCGAGA CCCCGCCCCC GTCTGCCTCC CTCCGGGTGG CTAAGCCGCA 600 CCTGAAGCCG CACCTGGTCG CAGAGGCTAC TGCTGGGGAA ACCGTTGGGC CAGCGGCGGC 660 TAAAGGGCAG GAGGCGCCGC TGTGGCCACG CGCACTTCTG ATTCCGCTCC AGGGTTTCAG 720 AAGGAACTGA GGGCTCTGGA CCCGGCCTCG GAGGCCTGAG GAGTTGGGAG GGGCGGCGGC 780 CGCGTCCTCC GCAACTCTGG GGAGAAGTCT TAGTTTCCGC GCAGCCAAAC GCGATTGGAC 840 CCCGCCCTCC GGCTTCACTG GGGACCGTGG GGGCGGAACC CGGCGGGAGG ACGTATGGGG 900 GGCTGGACCA TGATGGAGGG AGTCGGTTGG GCTGGACCTC GAAATGCCTC TGCTCGCTTT 960 CCTCTGCGCT TATGCCGCCA TGTACGAGTA TGCGCTGTTT CCAGGTGGTT TGTTATACAG 1020 CAGTAGATAA CTGATACATC CCTTTTCACT AATATTTTTA 1060
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