| Tag | Content |
|---|
EnhancerAtlas ID | HS093-00828 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:40425730-40426970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:40426047-40426067 | CCCCCACCCACCCCAATCCT | + | 6.6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34178 | chr1:40425200-40426993 | HCC1954 | | SE_64654 | chr1:40425188-40426196 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 40426773 | 40426921 | | chr1 | 40426208 | 40426621 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I039959 | chr1 | 40425449 | 40427071 |
|
Enhancer Sequence | CCTTGGATGA CGTAAATTAC CTTCTCCCTT GGTACAAAGC CTGTGCTACT CAGCTTCAGG 60
GGCAAAGTAG GCGGAGGTGG TGCCACGGAT CGGATCAGAC GGCAGGGGAG ACGCACAGGA 120
TAGGCTGTCA GGCGGGGGCT CTGGTTCCCT CCAGGACATC CTGCTTCAGG GTGTGGGGGG 180
GCATACCCCT TTCATCTCCA GCCCATCCAG GCTTAAGTGG GCGCCTTCCT GCCCCAGGGG 240
CGCCCATACC TGGCCTCCGG CCTTCAAAGC TCTTCCCGCA ACCCCTTCCC CCACTACAGC 300
TTCCTTTCCC ACGAGGCCCC CCACCCACCC CAATCCTGCC AGCCCCTGGC TAAGGCCCAG 360
GTTGGAGCCT TTGATCCAGT CTTCAGGGCC GGGGGCAGGA CAGCCTGCCT TACCTGTGCA 420
GGCTGCTCAG GGCTCCCCCG GCGCCAGCCC GTGAGACTTG GCCCTGTGCC CGCCTCCCTG 480
GCAGCCAGTA GAAGGGGAGG CTCTGCTGCC ACGTCGCCTC ATGAGGCCCA GCCAATGGGA 540
GGCAGCCGCT CCCAGGGATG GTGGCTGCAG GCCGGGTTAC TCCCAGTTAC ACTGGGTTCC 600
TCAGCAGCAG CTGCTCAGCT GCTTATGAGC AGAGGATGGA GTGTTTGACA AAGGCTGATG 660
AGGAGCTCTT GTTCCCTGAG GAGACAGAGT CAAGAGAGGT GGAGGTGGGC AGGCCTTCCC 720
TGTGGCATGT AGGAACTGAG CAACTTCCTG GGCAGGCGTG GCAGCCAGTT TGGGGAAGTT 780
GCTGGGGGCC CTTCAGGCTG GTTTCTGATC TAGCAGGTGC CTGTGTGCAC ATGCTTCTGT 840
GGCTGGTGGT GCCTGTGTAT GCCTGCACGC GGGATGGCTC GTGGGCTGAA GGCTGGTGTG 900
CATATGACCT CCCTGTCCAA ACTTTTTTTC CTTTTTGTGG TGAATGGGGT CTGGCTATGT 960
TGCTCAGGCT GGTCTCAAAC TCCTGGGCTG GAGCTATTCT CCTGCCTCTG CCTCCCTAAG 1020
TGCTGGGATT AAAGGCATGA ACATCACCAT GCCTGGCCAG ACCTCTCCAT CCATACCACC 1080
TGACCCCTCC TCAGGCCAGG CCTGGAGACC TGGAACCCCC TTTCCTTTCA GTGTAGGAAG 1140
AAACTGGGTC TGTCAGGGTT TGTGAACCCT GTAGCTCTCT CTCCTCCTGG GCCTCAGGGC 1200
AACCCCTGCT TTAAGCCTAC ATTTAAATCC TCTTCTTGAA 1240
|
