| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14212 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:72189020-72189970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr17:72189315-72189326 | AATGAGTCACC | - | 6.02 | | KLF4 | MA0039.3 | chr17:72189175-72189186 | GCAGGGTGTGG | - | 6.62 | | Myog | MA0500.1 | chr17:72189883-72189894 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr17:72189883-72189894 | CTGCAGCTGTC | - | 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 |
| GH17I074192 | chr17 | 72188958 | 72190342 |
|
Enhancer Sequence | CATACAACAC CCCTTATGGC TTCCCTCAAA TAATCACCCT TTGCCCCTGG TTTGCATAAA 60
ATCTCAGGCC AATCAACCAC AAACCAGAGC ATCTCTGAGT CTCAGTCCCA ACCCCAGGAT 120
TGTCCCAGGA TAGTCTAATC ATCTGAGGCC ATCAGGCAGG GTGTGGAGCT GGGAAAACAG 180
CCCATCTCCC AGGCTGGAGG GCAAACTCCA TCAGCACAGG GAACATGTTT CTTCATCTCT 240
AAGAGAAGAT CATGTTCTAG CTAAGAGAAG GTGCTTAGTA AATATTTGCA GAATAAATGA 300
GTCACCTCAC AGTTTGGGTC CTGCTCCGAC GAACACATGA CCCAGCTGGT CCCTGGAGAA 360
GGAGGCAAAG GCTTTGAGGC ATTCAATAAG GCAACGCTGC ACACTCAAGT CACGAGGCTT 420
CCTTGCCCTC CAGTTACTAG CTGTGTGACC TTGGGTGAGT CACTTAACCT CTCTGTGCCT 480
CAGAGGCCTC ATCTATAAAA TGAGGGTTTC AATTTTGCCT AACTTAGAGC CGTGGTGAGG 540
ATTACAGATG ATCTTCCTGG AACAGCTGGA GTGGCTCCTG GCGCATAGTA GACACTCGAC 600
ACAGCGGAAG CTGTTGTTCC CTGTTCTATG CTGAAACCAC AGGACAGGGT CCCTCTCTGC 660
TCCACCAGCA GGCTTCCTCC CCAGGTCTCA TGTGACTCCA GCCAGCCACA CACGCTGACC 720
CTCTGCCAAC CCAGCCAGAC CTCTGTTCTC AGGGCGTTAA ATGCAAGGGG AAGGCCACGT 780
TGACAACCAA CTGCAGCCAC GCCTCCTCTG CCCTCCCCAG GAGCCTGGGC TGAAGACTTC 840
ATCTGCTGTA ATTAACAAGC CAACTGCAGC TGTCTTGCTC CATTAATAGC AGATCAGCCT 900
GTCGGGCGAG GGCTGACAGG GAGGTTGTGA ACAGAAAGGT AAGAAGGAAG 950
|
