| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14618 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:139960120-139960710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr9:139960518-139960533 | CGACCTCTTGACCTC | - | 7.26 | | RARA | MA0729.1 | chr9:139960515-139960533 | AAACGACCTCTTGACCTC | - | 6.61 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 139960121 | 139960356 | | chr9 | 139960571 | 139960676 |
| Enhancer Sequence | CTGCAATACG TGCATTTACA TGGAATGCCT GGCCCCAGTG AGCACGCACA CGTCCACACA 60
TGCATGAGCT CACCTGTGGG TGGGCACCAG AGCCACAGAC ACAAATGCAG CAGCACGTGT 120
ACACGTTTGC AAACACCCAC GGACGCACGC TTCTGCTGAC ACCTGCATGT GTGAGCCCCA 180
TAGGCCCATT TGGAGCAGGA GCCCCGTTCC TCCTGCTGAG GGGTCTTGGC CTTTCTTAGC 240
CCCTCCACTC AGGCTTCCCT GGGGGAGGGG TGACGGACCC TTCAGCTGAG CCCACCCTCC 300
CGAAGTCTGC CTGTGGTGAG CACACAGCTG GGAAGCCAGA CTGGCTTGCA GCAGCAACCT 360
CGTGAGGCGG GCTGGGCAGC CACCATAGCT GCCCTAAACG ACCTCTTGAC CTCCCTCTGC 420
CTGACCCTGG GCCATCCCTC CAGGGGAGTC AAGCCCAGGT AGGGAGAGAG ATGTCCAGAG 480
CTGACTGTAC TTCCGCCATG GACTCCCCCA GGCTCAAGGC CCCCCTGCTC CCATCCCGGC 540
CTCCAGCCTC CAGGCAAGAT GGAGAGCCCC ACAGAGCCCC AGTCCCTGCT 590
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