| Tag | Content |
|---|
EnhancerAtlas ID | HS095-14003 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr18:55869260-55870100 |
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 | TTCCAATAAA AATAAGTAAA TTCTTCCTCT CTTGCCTTGA AGATGTGCAG CTCCTCAGTA 60
ACCTTTTATT CTCTAAAGCT CTGTCCTCAT CTTTAATCCC TGATTTAAGA GGTGCAGCTC 120
TTCAGGCCAT AAACCTTTCT TCCTGCCTCA AGTTTTTAAA GCTACAAAGG AACCTAAGAG 180
ATCCCTTGTG TTTTACAGCT AAAGGACCTG AGAGCAGGAA ACAAAGGGAG AGCCGGAAGC 240
CCAGGTCTCC TGTTCCCTGC CTGGCAGGTG ATATTCTTTC TGTTAAACTC TCTTTCCCTC 300
TGCCTATTAT TGGCCAGGCT GTCCTCCAGG ACAGTGCTTG CCAAAGTGTG GTCCATGGGC 360
AGCAGCATCC CCGGAGCTCA TCAGCAATGT AAGATGTCAG GCCCTGCCCC AGAGGGGCTG 420
AGATAGAATC TACCAATTAC TGGATTCCCT GGGTGACTCA TGCAGTCAGG TTGGAGAAGC 480
GCTGGACTGG TGGCTTTCTC CAGAGGAGCA TGCAACAGCG GTTTGCAAAC AGGGATGATG 540
CAGTTCCTTT TCAACACGTG GATTTGCACT TCCTCCTGGT GCGCTCCTCC AGCCTGCCTG 600
TCCTGTTCAC ACCAGCCTCC CCCTGGAAGG GGTTCAGACT TGATCCTTTG GGTGGTAGGG 660
TCTTTCTTGG ATAGCGTAGC CATCCATTCC TGCTGCATAC ATTCAACACA GCCTTCATCC 720
TTCGCCATTT GTCTCTGATA CTTCATACTC CTTTTGTTTG ACAAGTGCCC TAGCTTTATT 780
TATTTTCTCA TCATTGTTGT TAAGGGCCTA TTGTGCTTGC TAGTATACAC ACCACTATGT 840
|
