| Tag | Content |
|---|
EnhancerAtlas ID | HS184-27211 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr7:1233140-1234180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SNAI2 | MA0745.2 | chr7:1234035-1234045 | AACAGGTGCA | + | 6.02 |
| | | 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 |
| GH07I001194 | chr7 | 1233641 | 1233750 |
| Enhancer Sequence | GGTGAATGAA TGAACAGTGA GTTCACTCCA CATTGGGTGC CTCAGTCCAG CCGTCCCCGT 60
ACACCCGAGG GGCCCCACGC AGCCACACCT GGCTTTTCTC AGGCAGTGGC TCTTCCCACC 120
TGGGTCTCCG TCCTAGGGGT CTGTCGCCCT GATGTCAGGG AGCGGGCGCA GCTCTCAGAC 180
GCGCTGGTGT TGTCTCCTAA CTCTGCCGCT CCCCAGCTGT GTGGGCCGGT CTGCCCCAGT 240
TTCCTGCTCT GAAGAAGAGA GATTGAGATA CAGGTGGCAG CCTCGGAGGG TGATTGTGAA 300
GGGTCCAGGC GGTTCCCGCG TGCAGCCTCG GGACAGGGCT GTGCTGGAGC CATCGAGCTG 360
GAGAGAGAGT GAGCTTCACC CCAGGGCAGC TGTCTCCCCA GACGAGCCCC GCTCTGGGAC 420
ATTGCATGGG AATCTCAGCT GCTCCGGGAT GTTCATTCAC CCTACCTCTC TCAGGACACC 480
CTGGCTTTGC AGAGCCCGTG CGTGAGTGTC TCTGAGCCGG GTGCCAGGGG GTGGCACTGT 540
TTGCTCACCG TTGGCCTCTG CTGGCAGCGT GGTGCCCGGC GCGGCGTGAA AGCCCTCGGC 600
CTCCCAGGCG CTTTCGGCCT CACAGGCATC CCTCTGGCTC GAAGTGCTCC TGCTCCCACA 660
AGGCTCAGGA AACCTGTGCT GCTCAGAGCT TTGCGTTTAA AAATCACGTT GTTCTGGTTT 720
GGACCACGCA ACTTAGACAT TTCTTTCAGG AACTGGATTG GCTGTGGAGG GGCCATTTAG 780
AAATCTTTTA TCTAGTCAGT TTCCTTCATC TGTATTTTGG AAATGCAGAG AAGGTGATTG 840
AACCTAGCGG AATCTTGGGA GCATGTCCTT GAACACGGCA GGTGTCCCCG GGACAAACAG 900
GTGCAGCTTT CTGCAGAGGA CAGCGATGCC CCGGACAGCC TGGGCTCCCA AGTTCTCCCA 960
TGTGCCCCAA GGTGCCGTGC TAGGGTACAG GGGGTTGTGG AGTTTACTCA TTCCTGGAGG 1020
CAGGTATTCA GCCAAGATCA 1040
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