| Tag | Content |
|---|
EnhancerAtlas ID | HS007-08234 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr19:33901360-33902240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr19:33901882-33901894 | TGCCCCGGGGCA | + | 6.74 | | TFAP2C | MA0524.2 | chr19:33901882-33901894 | TGCCCCGGGGCA | - | 6.74 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCATGTGTG TTCCTGTCCT TCAGTGGGCA TGGCTGGGGA CTCTGGGGGG TGGGCTCCCA 60
CGACTACCTG CTGTAGGGTG AGGCGGGGTC CAGGCCGGTG AGCAGCCATC ATGGGAACTC 120
CCGCTGGAGG AGCTGGCACA TTGGGGTGGC TCCTCGATGG GAAGGCGGAG GCAGCCCAGC 180
TGGGCGCCAC GCAGGCCTCA GAGGACATGC CATGCTGCTG GGGGGCAGAG GGCTCTGCAG 240
GAGGCTTGTT CGGGTGCATC TGCCATAGAA GAAAGGGCAC CAAAGAACTG GGAGGGACAA 300
GGCACATCCT CTGCTAGTCA GTGACCACAG TGAAATGTCT GGAGGCCAAG ACAGGGCCTG 360
CGTGGCTGTG GCTGAGCCCC AGGGCTCCAG CACTGGGGTA GCTCTCAGGA GCTCTGCACT 420
GCCTGGGCTG GCCCTGGCTG ACATCTGACG TGCAGGGCAC AGGCAAAGAA CGCGGAGGGA 480
CTGAGCAGAG GCCAGGCTGC AAGTACTCAC ACACCTCCTC CCTGCCCCGG GGCAGCGGCC 540
CAGCTGCTCT GCCCTGCACA CCGAGGGGCT GTGGGTAGGA CTGCAAGTCC TCCAATGAGA 600
GAAAAGACTA CCCGAGGGGC GGAGGCCGCA GGGCCTGCCC ACATCTCCTT GTCGTGGCTT 660
CTATGAAGAA CTGTGAGCAC GGCACATCGT GCTCAGGAAA GCCCTGCACG CAGCCACGGG 720
TCAGCACTGC TGACTTGCTG AACGCAGGGC CGCAGAGGCC ACGGGCTCCT GCAGCAGGAG 780
GATGGCAGGT TTCAGAGCGT GGGAGGCTCC CTGCGGTCTT CCCAGCTCCA GACCAAGAGG 840
CCTGCCCTCC TGGCACCAAG ACAGAAAGAT GCGAGCGTGG 880
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