| Tag | Content |
|---|
EnhancerAtlas ID | HS116-16384 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr18:55869310-55870000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr18:55869711-55869722 | GGTGACTCATG | + | 6.62 | | FOSL2 | MA0478.1 | chr18:55869710-55869721 | GGGTGACTCAT | + | 6.14 | | JUNB | MA0490.1 | chr18:55869710-55869721 | GGGTGACTCAT | + | 6.32 | | JUND | MA0491.1 | chr18:55869711-55869722 | GGTGACTCATG | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27800 | chr18:55869040-55870289 | Fetal_Intestine | | SE_28643 | chr18:55868651-55870453 | Fetal_Intestine_Large | | SE_41571 | chr18:55869281-55870207 | 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 |
| GH18I058201 | chr18 | 55868921 | 55870489 |
|
Enhancer Sequence | CTCCTCAGTA ACCTTTTATT CTCTAAAGCT CTGTCCTCAT CTTTAATCCC TGATTTAAGA 60
GGTGCAGCTC TTCAGGCCAT AAACCTTTCT TCCTGCCTCA AGTTTTTAAA GCTACAAAGG 120
AACCTAAGAG ATCCCTTGTG TTTTACAGCT AAAGGACCTG AGAGCAGGAA ACAAAGGGAG 180
AGCCGGAAGC CCAGGTCTCC TGTTCCCTGC CTGGCAGGTG ATATTCTTTC TGTTAAACTC 240
TCTTTCCCTC TGCCTATTAT TGGCCAGGCT GTCCTCCAGG ACAGTGCTTG CCAAAGTGTG 300
GTCCATGGGC AGCAGCATCC CCGGAGCTCA TCAGCAATGT AAGATGTCAG GCCCTGCCCC 360
AGAGGGGCTG AGATAGAATC TACCAATTAC TGGATTCCCT GGGTGACTCA TGCAGTCAGG 420
TTGGAGAAGC GCTGGACTGG TGGCTTTCTC CAGAGGAGCA TGCAACAGCG GTTTGCAAAC 480
AGGGATGATG CAGTTCCTTT TCAACACGTG GATTTGCACT TCCTCCTGGT GCGCTCCTCC 540
AGCCTGCCTG TCCTGTTCAC ACCAGCCTCC CCCTGGAAGG GGTTCAGACT TGATCCTTTG 600
GGTGGTAGGG TCTTTCTTGG ATAGCGTAGC CATCCATTCC TGCTGCATAC ATTCAACACA 660
GCCTTCATCC TTCGCCATTT GTCTCTGATA 690
|
