| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15351 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:18430410-18431020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr19:18430643-18430653 | TTTAATTACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_11848 | chr19:18430248-18430936 | CD3 | | SE_22337 | chr19:18428282-18431470 | CD8_primiary | | SE_24690 | chr19:18430278-18432476 | Colon_Crypt_3 | | SE_28364 | chr19:18428061-18435342 | Fetal_Intestine | | SE_29445 | chr19:18428294-18435349 | Fetal_Intestine_Large | | SE_51038 | chr19:18428345-18435215 | Sigmoid_Colon | | SE_52930 | chr19:18428353-18435174 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGCAGACCC ACTCTCACAA CACTCCTCAG GCCCGCTATA GAGTCAAGGC AGACAGGCTC 60
TGCCACACTG GCCGCCACAC CCATTCCTGC CACCTGACCT TTGCTTCTGC TATTGCCTCT 120
GCCTGGGGTG ACCTTCCCCA GGCTGCTGAA ACGTCACCTC CTTTGGCCAG GCCCTTTTAA 180
TGGCCACCCT CTGCCTCATG GGTGTTTGTT TCCATCATAG GATGCAGCCA GTCTTTAATT 240
ACCTTGTTTA TTACCTGTGT CCCTCGCTAG ACTGGAACAC TCAAAGTGGG TGTGGACTTT 300
GTCCAGGGCC AAGCACAAGG CCAGGCACAT GAGAGGGACT CGGTAAATAT TTGCTGAATA 360
AATACACAAG AAAAATGCAC ACACTACCCA GGGAGGCATG CAGGGAAGGC AGAACACTCG 420
CCCCACCCCA CAGGTAAGGG AAGGAGTGGC TGCGGGACAG GGAGCTGCCT GACTCCCAGG 480
CCCTCCCAGG CTGCAATGGC CTGGGCCTGT GACCATATAT CTTGATTTCT CCTACATCCT 540
CATCTCCAAA CTCTGTTGGA GAGAGGTCAG AGGAAGGGGT GGATCCTCAA AATCTTAAAA 600
GAAGATACAT 610
|
