| Tag | Content |
|---|
EnhancerAtlas ID | HS139-05089 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:228999730-229000760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr1:228999832-228999843 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr1:228999831-228999842 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr1:228999832-228999842 | TCAAGGTCAT | + | 6.02 | | Myog | MA0500.1 | chr1:228999784-228999795 | CTGCAGCTGTT | - | 6.02 | | RREB1 | MA0073.1 | chr1:228999739-228999759 | GTGTTGGGGGTGGGGTGTGT | - | 6.16 | | RREB1 | MA0073.1 | chr1:228999730-228999750 | GGTGTGTGTGTGTTGGGGGT | - | 6.17 | | Tcf12 | MA0521.1 | chr1:228999784-228999795 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_49948 | chr1:228997517-229000847 | RPMI-8402 |
|
| | 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 |
| GH01I228863 | chr1 | 228999708 | 229000807 |
|
Enhancer Sequence | GGTGTGTGTG TGTTGGGGGT GGGGTGTGTC TAAGGTGATG CTGGGATTCT TACACTGCAG 60
CTGTTGTATC ACCAGCAGCA AGGATGATGG CGCAGGAGAC ACTCAAGGTC ATTGCGAGGG 120
GGCACAAACA CCTGGAGAAA GTAGCTCATC TTTGAGAGCA CCATGTGCTG CAGTATCATT 180
CAGTAGGACC TTTTTTTTTT TTCCGAGAGA GGATCTCTCT GTCACCCAGG CTGGAACACA 240
GTGGTACCAT CGTAGCTCAC TGCAGCCTCA AACCCCTGGG CTCAAGCATT CCTGCTACTT 300
CCAGCCTCCT AAGTAGCTAG GACTGTGTCA GCCAGGCTGT GCTTGAATAG TGAGATTCAG 360
GCATGGGCCA CAACACCCAG CTAATTTTTA AATTGTTTTG TAAAGATAGG GCCTTGCTGT 420
GTTGGCTTAG GCTCAATATA ACCTTTCTAT GGGACATTTA TTTGTTTAGT AAACTTTCTC 480
TGCCTCTCTC TCTCTGGTTT TGCTTTTAAC CCCAGAGGCC TAAGACTGAG TTGCTGATCT 540
TCCTGTTTTT GGCCCGATCA CACTCCTGAA AAGACTCTTT TAACTCTCAT TTCCTGCTCC 600
AGCCCCGTCC TCCCATAGGC AGCTTGCTGC AACCTGCTGT GGCTGATCCA CTGGGTGGGC 660
CCGAGCAATG GCTGCATTTC TAGTAGGGGG AGTTCTCCTT GCCACAGGAG ATCACATACA 720
CACTCCCTAG GCTGAGCTCA GGAATGCAAA CTCAAGTCAG CCTAACAGGG TGAGGCTGTC 780
CCATAGGAAG CAACATTTAG AAAAGAGTCA GGCCAGACTG GATTCCAACC CTGCTGGGTG 840
CAGATGGCTG GTCGGCAATG CCCCACAGCT GTCTTGGCCT TCCATGTGGA CTGCTGAGGC 900
TTCACATTTC CCCTTAGTAA CACAGCTGGG GCATTGCAAG GGGGTGGGGT GGGGGAGCTG 960
AACTGCAGAG GACTCACCTT CTGTGGGAGA AGATGGAAGG GAGGGGAGAT AAAACCGCAG 1020
CTGACTATAT 1030
|
