| Tag | Content |
|---|
EnhancerAtlas ID | HS091-43810 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:50682580-50683900 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr7:50683446-50683457 | CTGCAGCTGTT | - | 6.02 | | RREB1 | MA0073.1 | chr7:50682762-50682782 | ACCCAAAACACCCACTTCCC | + | 7.61 | | Tcf12 | MA0521.1 | chr7:50683446-50683457 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41576 | chr7:50681779-50682767 | LNCaP |
|
| | 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 |
| GH07I050613 | chr7 | 50681368 | 50684228 |
|
Enhancer Sequence | TGACAACACT GGCCAGGTTA AAGTCTCAAG CACAGCAAAG AGCAAATGTG TTCACCTCTG 60
GTAGACAGAG GGCAGTCTCT GCACACTTAC AAGCACTTTC CCCGATGACA CTATACATAT 120
TACATATGAT TATTACGCGA GGTGTAATAA GTGCTAAACT AAAACCAAAT TCACCCAGTC 180
TCACCCAAAA CACCCACTTC CCCAGTTCTC AGACACACAA GGCTGTTGGA ACGTATTTGA 240
TACTTCTGGC AAATCAAAGC CCCATGACCG GATATTCAAG ATAAAAAGCA GGAGAAAATC 300
TATAACCCAA AGGTCAGAGT TAAGAGCACA GGGCCTGTCT GCCTTTGGTT TGTTGTGAGT 360
CCAGAGTCCA ACCGTACTTT GGGTTTTCCC ACTGGTAGCT TGCTTGTCCC ACCCTTCTCC 420
TCCTCAACTC TCCAGCCCAG CTCTGTTTCC TGCTCTACGA AATACCCTCC CAACTTCAGC 480
ACACACGAGG ACAGTGAGCG GGCCACACAG CAGAGCTGGG AGGTCAGGAA GCTACCATGC 540
CCTGTGTCAG TTCAAAGCCC CTCTCTGCAG ACGCCCCTTC TCTCTGGCCC AGGTGTCGGC 600
AGCTGCTGAC TTCCCAGAGC CGGCCCCAAC ACCTTCCCAG AGCCGGTTCC CAGATGCTCA 660
ACACCTGTGC TGGGGTCCCG CCAGCTCCCT TTCACCTCTG CTGGCCAGAG CAAAAGAGAC 720
CACAGCCCTC AGATGGTAAG TGCTCAGCCA GGTATTGGGT GGACAAGGCT CCTGCCACAG 780
GGTATATGTG GACAGCACAA GAAGAGAGCA GACAAGAGTG TACATGGGAG CAAAGGAGCC 840
TCCGGCCTAA GCTCTCTTTT GAGGGCCTGC AGCTGTTTTC CATCTCCCAC CTTCTTCTCA 900
CTGGGGATAC ATGCAAGCCT GCAGTTTATT TCATGAAATA TCTATGATAC ATAAAGTTAC 960
ACTGGCATTA GGGTGGCAAT AGTCTATCAA ACATCTTTAC AGCTAGCTTA AATCCCAACT 1020
TATGAGAACT AGGCCAGTCT CTGAAGTGAT GGGGCAGCCA GGGGTGTCTG CTCCCAACCC 1080
GCAGTGGGGG TGGGGCTAGG CAGGTGGGGT TCTTAGGCCT GTATTATTTA TTACCTAGTT 1140
TCTGAGCGAG ACCAGGAAAC CTGTGACTCC AAGTTCAGCT GCTGCACAAT TAGCTTATTA 1200
AGAAGTTGTC CTGAGCTTGG AGGAGTCTAA GGTGCATTTA AAAATGAAGC CCAGGTTCAC 1260
TCTGAGGACC TGGGGGGAGT GACTGTGGCA GAATTAGGGC TGGTGGTGGT AGCTTTTAAA 1320
|
