| Tag | Content |
|---|
EnhancerAtlas ID | HS077-05563 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr19:5045840-5047120 |
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 | AAGCTCCTGA CCTCAGGTGA TCCACCTGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGC 60
GTGAGCTACC GCGCCTGGCC ATCTTTTTCT GTTTTTTAAC CATGCTGTTT GTTTTCTTCT 120
GGTTAAATTT GAGAGTTTGC TGTGTATTTT GGTTATCAGT TGTGACTTGC AAGTATTTTC 180
TTTCTGACTG GGGCTTGTCT TTCTCTTACG GATCCTGCCT GATTGTTTTC AAGTGAAAGT 240
TCAGCCTCAG ACTCCAGTGC ATGAGAGCCT CTGGGTTGGC TGGCCTGCAC TGCCTGCACT 300
TGGCCTGTAG TGATGACCCG GGAGGGACTC TGCAGCCGCA CGCAGGCTGT GCCAGCCCAG 360
GCCGACCTGC CACAGGTGCC AGGGGAAGCT TCAGGGCTTC CTTGCCATGT GTTTGCCATG 420
CCTAGCCTAT GCACTAGCCT ACTTTTACAG CGGGGGAAAC AGCCCACAGC AGAGAAGCGA 480
CTTGCTGTGG TCCCAGGATG AATTTGCGCC CAGCTCAGCC TGTGCCTGGG GCCTCCCTCT 540
GCCCCATCTG GGTCTCATCA CTGCCTCCCT CCTCACCTCT TCTGGGCTCC TGCCAGGGCT 600
CACCTTGCAA AGGAACCGCT GGTCTTGCCA AGTCTGAGGG CCGGTCGTGC AGGTGCAGGA 660
ACAGCTGGTG GGGGGTGGAT TCAGGCTGTG AGAGCAGCTC ACGTTCATGT GTGTCTGGGC 720
TCCTCTCGGC CTCTCAGCAG GCCATGAGCC TCTCCGGGGA CTGCAGTGAC TAATGTGTAT 780
TTTATGAGCT CTTGGGACAG GACGGGGTTT GTTTGCTTGT GGCATTAAGA ATAGATGTGC 840
CTGGTGGGTG GGGATTCCGT CCTTGTTTGC CTAGTTCTGA AAACTGTCTT CGTCTCCTCG 900
GTCAGAAGCT GTGGAAGGGC TGTCACTGGG CCTTGGCTCC GGTACCATCG CTGGGTTAGC 960
CCCAAGTGGT GACTGTTTTT CTCCTTCCGT GTCATTGACT TAGAGGCGTG TTAATTATGC 1020
ACTCCCAAAC TGCAGGCTTC ACAACAAGGC CTCCACCCAG CAGGAAGCAC GCAGCTCAGT 1080
GGAATCTGAC AGGCCCTGCC TGCCTGGTGC ACGCTGGCAT GTGCGATGGG GCCCTTCCTG 1140
GAAGGGCCAA GCTGGCGGTG AGCCCTTCAG AAAAGGTGTC TGGGCTGGGT ATGGCGGCTC 1200
ATGCCTGCAG CCCCAGCGCT TGGAGGGGCC AAAGTGGGAG GGACCATTGA GCCCAGGAGT 1260
TCGAGACCAG CCTGGGCAAC 1280
|
