| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15095 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:5045920-5047150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr19:5046496-5046509 | AGGAACAGCTGGT | - | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41729 | chr19:5045841-5049299 | LNCaP | | SE_65334 | chr19:5045698-5050618 | Pancreatic_islets |
|
| | 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 |
| GH19I005045 | chr19 | 5045762 | 5050235 |
|
Enhancer Sequence | ATCTTTTTCT GTTTTTTAAC CATGCTGTTT GTTTTCTTCT GGTTAAATTT GAGAGTTTGC 60
TGTGTATTTT GGTTATCAGT TGTGACTTGC AAGTATTTTC TTTCTGACTG GGGCTTGTCT 120
TTCTCTTACG GATCCTGCCT GATTGTTTTC AAGTGAAAGT TCAGCCTCAG ACTCCAGTGC 180
ATGAGAGCCT CTGGGTTGGC TGGCCTGCAC TGCCTGCACT TGGCCTGTAG TGATGACCCG 240
GGAGGGACTC TGCAGCCGCA CGCAGGCTGT GCCAGCCCAG GCCGACCTGC CACAGGTGCC 300
AGGGGAAGCT TCAGGGCTTC CTTGCCATGT GTTTGCCATG CCTAGCCTAT GCACTAGCCT 360
ACTTTTACAG CGGGGGAAAC AGCCCACAGC AGAGAAGCGA CTTGCTGTGG TCCCAGGATG 420
AATTTGCGCC CAGCTCAGCC TGTGCCTGGG GCCTCCCTCT GCCCCATCTG GGTCTCATCA 480
CTGCCTCCCT CCTCACCTCT TCTGGGCTCC TGCCAGGGCT CACCTTGCAA AGGAACCGCT 540
GGTCTTGCCA AGTCTGAGGG CCGGTCGTGC AGGTGCAGGA ACAGCTGGTG GGGGGTGGAT 600
TCAGGCTGTG AGAGCAGCTC ACGTTCATGT GTGTCTGGGC TCCTCTCGGC CTCTCAGCAG 660
GCCATGAGCC TCTCCGGGGA CTGCAGTGAC TAATGTGTAT TTTATGAGCT CTTGGGACAG 720
GACGGGGTTT GTTTGCTTGT GGCATTAAGA ATAGATGTGC CTGGTGGGTG GGGATTCCGT 780
CCTTGTTTGC CTAGTTCTGA AAACTGTCTT CGTCTCCTCG GTCAGAAGCT GTGGAAGGGC 840
TGTCACTGGG CCTTGGCTCC GGTACCATCG CTGGGTTAGC CCCAAGTGGT GACTGTTTTT 900
CTCCTTCCGT GTCATTGACT TAGAGGCGTG TTAATTATGC ACTCCCAAAC TGCAGGCTTC 960
ACAACAAGGC CTCCACCCAG CAGGAAGCAC GCAGCTCAGT GGAATCTGAC AGGCCCTGCC 1020
TGCCTGGTGC ACGCTGGCAT GTGCGATGGG GCCCTTCCTG GAAGGGCCAA GCTGGCGGTG 1080
AGCCCTTCAG AAAAGGTGTC TGGGCTGGGT ATGGCGGCTC ATGCCTGCAG CCCCAGCGCT 1140
TGGAGGGGCC AAAGTGGGAG GGACCATTGA GCCCAGGAGT TCGAGACCAG CCTGGGCAAC 1200
AGAGTGAGAC TTCATCTCTA CACAGAAAAA 1230
|
