| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12945 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr16:90148260-90149110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr16:90148335-90148348 | CCATTGACCTTTG | - | 6.2 |
| | | 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 |
| GH16I090081 | chr16 | 90147961 | 90149608 |
| Enhancer Sequence | CCACTGCCTC TCCAGCCTGG GCTACAGAGC AAGCCTCCGT CTCTAAAATA AGAAAGAGAA 60
AAAGAAAAAG AAAATCCATT GACCTTTGTC TACTGGCCAT CTATTTTACT TGTTAAAAAT 120
CTCCATGCGT TCTGATCAAG GCATGTGATG GTGGGCTCGA TTTCAGTTGA AATTTCCAAA 180
ATCATGGCCC GGAGTAATCT GGAGGCTGAA TTTCAGAGAT TCCCGAGGGC TGCCGCGAGG 240
GGGCGCCCAG CCCCTGCTAA ACCCGAGCGC TGCGCGCTTG AGCCGTATCT GATCCGCAAG 300
GCGGCGTTGC GGGGCGTTTA CCGTGAGGAC AGAGCTTCCT CCCTCAGGAC GCGGCTGGGA 360
GAGGCTGCGG CCTCGGGAGA CATGGGGACA CTTGGGGCCG CGTCCACAGT GAGACAGGGA 420
GACGCTGCTG CAGCTTCGGG ACACCTGGGG CCGCCCAGGC GAAGATGAGG AAAAAGCTTC 480
CTGTTGCCGT TGAGTGTAGC GGCGGGAGCG CGGCCGTGTT TCCCTGTCCG CCGTTTGTAG 540
CAGGACCTCA CTTTATATTA ATAAAAGCGT CCCCTCATGA GGGCTTGGGC TGGTCACCCC 600
CAGCGCAGGC CAAGATGCAG GTTATGGATG TGAGTTTGTT TCTGGGGAGA GACCCTGGTA 660
CCGGGAGAGG AGACGCGGTC AGGAGGCTGG GGACGGGAAG GCGCCACAGC CTGAGGCCGA 720
GAAAACAGGC GCCCCCGGAT CAGTGCTCGT TTTTTTTGGT TTGGTGTGTG TGTGTGTGTG 780
TGTGCGTGTG CGCGTGCGCG TGCGTGTGTG TGTGTGTTTT GAGACCGAGT TTCGCTCTTG 840
TTGCCCAGGC 850
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