| Tag | Content |
|---|
EnhancerAtlas ID | HS002-04709 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr18:55868900-55870030 |
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 | | NR3C2 | MA0727.1 | chr18:55869023-55869040 | TGGTACATACTGTTCTG | + | 6.03 | | Sox6 | MA0515.1 | chr18:55869203-55869213 | CCATTGTTTT | + | 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: 2 | Chromosome | Start | End |
| chr18 | 55869037 | 55869309 | | chr18 | 55869311 | 55869996 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I058201 | chr18 | 55868921 | 55870489 |
|
Enhancer Sequence | CTTTCATCCC TGCCCCCTAA TAGGTAACTG TCTTTATTTG TTCTGGGATT ATCCCTCCTC 60
CATTGCCCTT TTTGGAAAGA GTATGGATAT ATTTGTATTT TCTCTTACTC ATAAAGCAGC 120
ACATGGTACA TACTGTTCTG AGCCCTGGTT TTCTTTTTTT CACTTAGCGT TGTATACTGG 180
AACTCACTCA ATGTCAGTAT ACAGAGAATT CCCTTGTCTT TTTATAACTC TGTGCTATAC 240
GCTGACGGAA GTTCATTCAG TCAGTCCCCT ATTGATGGAC ACTTGAGTTA TTCTCAGACT 300
TGTCCATTGT TTTGCAAAAA TAGCCCTGGG CATATGTCAT TTGGTATTTT TGTCGAGGCA 360
TTCCAATAAA AATAAGTAAA TTCTTCCTCT CTTGCCTTGA AGATGTGCAG CTCCTCAGTA 420
ACCTTTTATT CTCTAAAGCT CTGTCCTCAT CTTTAATCCC TGATTTAAGA GGTGCAGCTC 480
TTCAGGCCAT AAACCTTTCT TCCTGCCTCA AGTTTTTAAA GCTACAAAGG AACCTAAGAG 540
ATCCCTTGTG TTTTACAGCT AAAGGACCTG AGAGCAGGAA ACAAAGGGAG AGCCGGAAGC 600
CCAGGTCTCC TGTTCCCTGC CTGGCAGGTG ATATTCTTTC TGTTAAACTC TCTTTCCCTC 660
TGCCTATTAT TGGCCAGGCT GTCCTCCAGG ACAGTGCTTG CCAAAGTGTG GTCCATGGGC 720
AGCAGCATCC CCGGAGCTCA TCAGCAATGT AAGATGTCAG GCCCTGCCCC AGAGGGGCTG 780
AGATAGAATC TACCAATTAC TGGATTCCCT GGGTGACTCA TGCAGTCAGG TTGGAGAAGC 840
GCTGGACTGG TGGCTTTCTC CAGAGGAGCA TGCAACAGCG GTTTGCAAAC AGGGATGATG 900
CAGTTCCTTT TCAACACGTG GATTTGCACT TCCTCCTGGT GCGCTCCTCC AGCCTGCCTG 960
TCCTGTTCAC ACCAGCCTCC CCCTGGAAGG GGTTCAGACT TGATCCTTTG GGTGGTAGGG 1020
TCTTTCTTGG ATAGCGTAGC CATCCATTCC TGCTGCATAC ATTCAACACA GCCTTCATCC 1080
TTCGCCATTT GTCTCTGATA CTTCATACTC CTTTTGTTTG ACAAGTGCCC 1130
|
