| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08858 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:132662940-132664260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr12:132663148-132663162 | TGTCCCTTGGGATT | - | 6.24 | | Gata1 | MA0035.3 | chr12:132663975-132663986 | TCCTTATCTGT | + | 6.14 | | KLF16 | MA0741.1 | chr12:132663670-132663681 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr12:132663670-132663680 | GCCCCGCCCC | + | 6.02 | | Myod1 | MA0499.1 | chr12:132663005-132663018 | TCCAGCTGTCCCT | + | 6.16 | | SP4 | MA0685.1 | chr12:132663667-132663684 | CGAGCCCCGCCCCCTCC | + | 6.16 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr12 | 132662941 | 132663228 | | chr12 | 132663524 | 132663727 | | chr12 | 132663332 | 132663875 | | chr12 | 132664166 | 132664206 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132178 | chr12 | 132662746 | 132663750 |
|
Enhancer Sequence | TTCTGACTTT TTTCGTTTTT GAAATCGTTT CCGGCTGGCC CAAGTCGAAA AATAATGCAG 60
ATGTCTCCAG CTGTCCCTGA GAACACTTCC TGTTCCTTGA TCTGTGGCTT GTGATTCTCC 120
CCCCGCCCCC ACTCCCCTTA CATGGGGCTG TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC 180
CTCAGGATTG TATGACTGCA GGTTGGGCTG TCCCTTGGGA TTCAGGGCCT CAAATGTACC 240
TGCTGACCAG TTGAAGAGTG CTGACCAGCT GTCCTGCTGA ACACCTCTCA ATCTGGATTT 300
TTGACATTTC CCTGTGATTA AATTCAGGGA ATCCAGCTTT GGTGACAGAG CCACTGAAGC 360
AAGGCTGTTC CCTGCTTGGA GACGCACCCA CTTTACACGT GTAGGGTGGC GAGTCTGACA 420
AACGCAGCCA CAGGCAGCCC CCACCGGGGG AGCCGGACGT TTCCATCCAC CCAGACAGCA 480
GCGTTCACGC CCAGGACCAT GTGGGCCTGC GCCCCGGGCC GCACCTGCCT CTCCTGCATT 540
CCGTGTCTGG CATCTTGTGT CGTTGCCACC CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA 600
GCGAGTGTCC TCCGTGTCTC CGAGTCGCGC CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA 660
GAGCTGTTGT TTGTTTAGGG ATGTATCATG TTTTCAGCTT AACATTTGTG CCATTCGTGT 720
GCCCTGGCGA GCCCCGCCCC CTCCAAGTTA CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT 780
ACTCTTCCTG CTGTCGCCAG CGCAGCCGAA GCACCAAGCA GGAAGCTCTG CCGAGTTCTT 840
GGCTTCAGGT AACGTGTCAG ACCCAGGGCA TGAGCTCCAG TCCCTCTTGC CTCCACAAAG 900
GACAGCACAT TTCCAGTTCA GGGTGCTGTG GCCGACACCG TGCGTGTGGC TGGGGCCAGT 960
GTCACCGCGA ATCTCGGCTG CTCCACGCCC TTGCTGTGGG CTTGGGGCCA GTGCTTTACC 1020
TCTCTGGCCT CAGTTTCCTT ATCTGTTAAC AGGGTTGGTG TGAGAATGAA TGAGAAGGCA 1080
TGCACAAAGC GGGGCACAGC CTGCCCCAAA GCAAGGTCCC GATCCAAGTA GCTGCCGTTA 1140
TTGCTAATAG TGGTCCCAGC GGAGCCACAG TTGCTGAACG GTCCTGCAGA GATGTCCCCT 1200
TGGGTACAGG GCCCCCAGGG AGGAGCTGGG GACAGAAGGC AAAGCAGCTG GATCCACCCA 1260
TGCCTGCAGC TTGCTCTTTG CTTAACTGGT TGTTAGAGTT GTCTGTGCAA TGGCTGATGG 1320
|
