| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08705 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:121661260-121662000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr12:121661829-121661842 | TCCAGCTGTCCCT | + | 6.16 | | ZIC1 | MA0696.1 | chr12:121661509-121661523 | CACAGCGGGGGGGC | - | 7.19 | | ZIC3 | MA0697.1 | chr12:121661508-121661523 | GCACAGCGGGGGGGC | - | 7.39 | | ZIC4 | MA0751.1 | chr12:121661508-121661523 | GCACAGCGGGGGGGC | - | 7.39 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_19765 | chr12:121660407-121663031 | CD4p_CD25-_Il17p_PMAstim_Th17 |
|
| | 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 |
| GH12I121222 | chr12 | 121660450 | 121662897 |
|
Enhancer Sequence | TGTTGTGGCT TTTTGTGTGT TTCTGGTGTC TGTATGAAGT CAGGCTGCCC TAGGATGGCT 60
GCTCTCAACC ACAAGGCAGC GACCATCAGT GGCAAGATGG GCCACAAGTA GTCTGTCACT 120
CACGAGAAGG GTGCAGGTGA CTGACTTCCT TGTATGTTAG GACTCTGTCA GTTGCAAATA 180
ACTGACAGGA AACAGTTCTC AGTGCCTTAA GCACATGTGC ACAAACACAT ACACACATAC 240
ACATGCGTGC ACAGCGGGGG GGCAGTGTAT TGTCCGGCTG ACCAAAAAGA TCCAGCGTGG 300
CCAGGAGAAT CTCGTGCCAG GCTGAGGCAG AAGAATCTCT TGAACCTGGG AGGAGGAGGT 360
TGCTGAGCTG AGATGGTGCC ACTGCACTCC CTCCTGGGCG ACAGAGGCCA CTGCACTCCT 420
GCCTGGGCGA CAGAGTGAGA GACAAAGGAC AACACCCTAG TCTCCCTTCC TGGCTCTGCA 480
TCCCGCCGTG CCAGCTTCAC TCGCAGGACC CACAGCATAG CCCGGGAGGC AGCGCTGCAC 540
TTACAGCCCC CCAAGTCTGA GTCTCCCTTT CCAGCTGTCC CTGGAGATTC TAGACCTGTC 600
CATCATCGTA TCAATGGCCA TATCTCTCAA CCCATCTCTG TGGCTGGGGA ATGGGTTTTG 660
CTTATCAGCT TGGGCCTGGG TCACATGCCC ACCTCTGCAG CTGGGGCTAG AGTCAGACCC 720
ACCCAAGTGA CATAGGCAAG 740
|
