| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14947 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:883440-884360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr19:884099-884111 | CCCCACGTGCCC | + | 6.07 | | MYC | MA0147.3 | chr19:883478-883490 | GGGCACGTGGGG | - | 6.07 | | ZEB1 | MA0103.3 | chr19:884091-884102 | CCCACCTGCCC | + | 6.14 |
|
| | 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 |
| GH19I000883 | chr19 | 883600 | 884759 |
|
Enhancer Sequence | AAGAGCTGGG CATGGCGGGG ACCAAAGCCT GGCATGGTGG GCACGTGGGG CGGTAGGGGG 60
AGAGATGGGG GAGAGATGGG TGCGGTGGGG ACTGTCCCAG TGACCCCCAG CTGCCAGGGA 120
TGTGAGACCT GAGAAAGGCT GTGGCATGTG TGTGAGACGT GGCTCTCGGG CGGGTAACAG 180
CTGGGCCAGC AGGTGAGGAC GGCTGCAGGA GACGAGGAGG AGTGTCGGAG CCCAGGACTG 240
CCCAGTGGCT TGGCTGTGGG CAGATGGTAG ACACAGACGT GCCCAGCGGG GGCACCGGGC 300
AGTGAAGGTG CAGGTCTGTG CAGCCACACG GGGTGGCGCC AGGTGCTGCT GCAGGAGCCA 360
GCGCAGCCCA AACTGCCTGG TGACTCACCA CGAGGCCCAG GGGAAGGAAT GAGGCCCAAC 420
AAGGCCCTGG GGACCGGGCG AAGGAACGAG CCCTGGGAGA AGGAATGGCA GCAGCCCTCT 480
TCACCTGCCT GGTGACTCAC TACAAGCCCT GGGGGAAGGA ATGGCAGTGG CCCTCTTCAC 540
CTTTACTGCC TCTGCGGCCA CAATGGGCAG TTGACATAAC CACCTGCAGG CCCCGGGAGC 600
CATCGGGGCC TCTTGACACG TGCTCATTAG TGGCTTCTGA GGAGCGCCTG CCCCACCTGC 660
CCCACGTGCC CCCACGTCTG GCCACTCCAG GGTCCATTAG CGCTAATCGG CAAATGCCTG 720
TGCTCTCATC TACCGGGAAA ACATCTCCCT TCTCCAGAGC GGAGGCCAGC CTAAAAACCA 780
GGCCCGCAGC CTCCGAGGCT CTGAAAACCA AGCGGCTGTT CTGGTCCCCG GTCATAGCAG 840
GCGGGCGTCC CTGCTTCGCT CCAGCCCCAG GATTTTGTGC CGGAGGTGGG GATGACGGGC 900
TTGGCTCCGT GGGTGCGGGG 920
|
