| Tag | Content |
|---|
EnhancerAtlas ID | HS098-19698 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:65010270-65011380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr15:65010520-65010538 | GTGAGGAAGGACGGAAGG | + | 6.56 | | EWSR1-FLI1 | MA0149.1 | chr15:65010524-65010542 | GGAAGGACGGAAGGAAGT | + | 8.13 | | HSF1 | MA0486.2 | chr15:65011210-65011223 | TTCTGGAACCTTC | + | 6.33 | | NFIC | MA0161.2 | chr15:65011238-65011249 | TTCTTGGCAGA | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_54599 | chr15:65009844-65011549 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH15I064716 | chr15 | 65008779 | 65011573 |
|
Enhancer Sequence | AGCATTTCCA CTCGTCTGCC AAGGCAGAGA CAGCCCCATC CAGAAGCAAG AATGAGACCT 60
CGGGGCCCTG GCGCCCTTGA GCCAACCCCA TCTCTGTTCT CACAACTTGC CTTGCCTGAC 120
CTCTGGAGAA AAACTTCAGA AAATATCACC CTTTCTTCCC ACCTGCTCCC GCTGGCCAAA 180
ATCCCCATCA AAGCCTGGCT TCAGCCCCTC AGACTGGGAA CTCTATCCAA ATGGAGTGTG 240
GGGAGTGTGG GTGAGGAAGG ACGGAAGGAA GTAGGTCACA CGCTGGCTAC CGCACAACGG 300
GGAAGAGGCC AACCTCGGAA AGGCAGAAGA GTGGCCGCCA TGCCGAGCTT CCAGAGATGG 360
AGAGAAGGTC TAGGAAGCCA CCTTGGGGAA GCCGCCTGAG CAGGAGCGGG GCAGCCAGGG 420
ATCAGAGCCC ACGGCCTGCT GGGGACCCAT CCTGGGCACG GGGCTCTGGG CTCTGTGCCC 480
ATTCTCTGAT GTGCCACATT GTTCTGCTAC TTCCTTCTCT GGAAGTAATA AGGGGGTTGG 540
GGGTGGGACA GCACGGCCAG GAGTAGATGG AGCGGGGTGG AGCTGCCAGT GGGGGAGGAG 600
GCTGCGGTTC ATTCCCACGA CCAGCTGCCC TTCTGGCCGC CCTGGGACTG CGTGGGAAAA 660
GGTCTGGGAA GTATGGGGGA TGGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 720
GTGTGTTTTC ATGTGTCTGA CTCCCTTGCT TGGCTTCAGT CACAGGACAA AGCCCTTTGA 780
GAAACAGTCA CCAACCTGTG TTCCCACTGG GCTCTGTCCT GGGAGAGGCA CAAGAACCCG 840
CCCTGACGCC TGAGAGAAAG ACTCTGAAGG CCTCAGGACC AAATCCCTGG AGGGGTCTTG 900
GCGTCTAATG AATCTAGATT GACTGACTTC CCTGGGATGC TTCTGGAACC TTCTGCTAAG 960
CCCTCAGCTT CTTGGCAGAG CTCTATTACT AACTGGATAT CAGAATATGG GTGCAAACTA 1020
GACATGGGGA GTGAAGTCAG CCATTCTCAC AGCATCTACC TAAGAAGGCC AGGATCCTCC 1080
ACAGCCACGT AGATCGTAGA GCCAGTGGCA 1110
|
