Tag | Content |
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EnhancerAtlas ID | HS194-04802 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr5:131725110-131726000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr5:131725569-131725580 | GATGAGTCACC | - | 6.32 | FOSL2 | MA0478.1 | chr5:131725453-131725464 | ATGAGTCACCC | - | 6.14 | FOSL2 | MA0478.1 | chr5:131725570-131725581 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chr5:131725453-131725464 | ATGAGTCACCC | - | 6.32 | JUNB | MA0490.1 | chr5:131725570-131725581 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr5:131725569-131725580 | GATGAGTCACC | - | 6.62 | Mecom | MA0029.1 | chr5:131725951-131725965 | TGTTATCTTATCCC | - | 6.12 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26597 | chr5:131723314-131726622 | Esophagus | SE_54554 | chr5:131720956-131726150 | Stomach_Smooth_Muscle | SE_62219 | chr5:131721125-131837948 | Tonsil |
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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 |
GH05I132384 | chr5 | 131720053 | 131726700 |
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Enhancer Sequence | AGTTACTTTC TGGAAATGTG GAAGTGGGAT GTGCTCCTCC TGGGATGTCC ATAAACGGTC 60 CTGGAGTCAG GGCTATAGCC TAGATGTCCT TACCAGGTTC CCACTAATGA GGCAAAGTAT 120 GTCAGAAAGG GATTTGTGAA TTACCAGGGA GAGGAAACAT GTCCAAGTGC ACATCGCTAG 180 CTTTTGCTCA GCGGCCGAAC CCTGGGATTC TAGGCGACTT CTGGAGCCTG GTGGGTTAGC 240 GGTGAGAAGA TGGGCGAGGA GGGCGGACTT CATCTCAGAG TCCTTATTAC TAGTCTCATC 300 CAGCTTTGAG GCAGTCAGCC ACTGTGCCTA CTGAGGGAGT GCTATGAGTC ACCCGCTTCC 360 AAGGAATGGC CCAGGATCCC TCCAGGCAGT TCACCATTCC CTGAGTTGGC CTCAAGACAG 420 GAGCAGCATG TAGCCTGCAC CACAGACATG CAAGCCTGTG ATGAGTCACC CACTTTTGTG 480 TTCACCCAGG CTCTCCTCCC TGCTCTGGAT TTCCTGGGGA CTCATGCACA TACTCTTTTT 540 ATTGTACCAG CTGTGTGTTC CACCTGCAGA TGAGTCAAAA CAGTCTAATC CATAAAGGTC 600 TGGTTTGTCA AAGAGTGTGG GTCATCAACA GAGAGAATGC CTACTGGGGA TGCCCAGGTC 660 AGGGGTACTG CAGGGCATCC TGATGAGAGG CAGTGTGGCC CCTCCATTGG GAGCCACCTC 720 TGTGCTCCAC AAGTACCGCG GGGCTGGTGT CAGCTGTCTC TGACCAGCCT CTTCCTGACT 780 GGTCACCACA GGTAGTGTGT GAGGGTCTCT CTCCAAGTGT TTGACCTAAT GTTGTTCCTT 840 TTGTTATCTT ATCCCCCAAA TCCTATCACA CCTCACTTGA TGTCTGCCTC 890
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