| Tag | Content |
|---|
EnhancerAtlas ID | HS093-01513 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:110044280-110045300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:110045108-110045128 | AGGATGTGGGTGGTGGGTGG | - | 6.38 | | RREB1 | MA0073.1 | chr1:110045119-110045139 | GGTGGGTGGGTGGGGGGTGT | - | 6.55 | | RREB1 | MA0073.1 | chr1:110045115-110045135 | GGGTGGTGGGTGGGTGGGGG | - | 8.93 |
|
| | 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 |
| GH01I109497 | chr1 | 110040120 | 110046097 |
|
Enhancer Sequence | TTAAAGCAGA TACCCAGTTA TCTCATGGTG CTTTCTAAGG ATGCTCAGTT CTGCTCAGGC 60
CCCCCAAAAG CAAACTATGA CCAAGTGAGG GAGCAGTGGG AGGTAAGGGA AATGCAGCAC 120
AAAGTACAAT CCAACTCCAG TACTTGCCAA CCTGTATGTG TGCGCACATG CACGCATACA 180
CCAGCCTTGG AGGCAATGAC TCCTGCCTAA TGTATGCCAG TGCCAAAGGG CATCCAGAAG 240
TCCCACTGCA GGGCTCCACG TCCTGGCTCA CTGCAGGTTG GTTCTCTCAG GCCATGGTTC 300
CAACCAGGGA GAGTAAACAA GCTGACTAGA TTGGAGGCGT CAGGGCAGGT CTAAGTGTCT 360
TCACCATTTT GCATTTTCCA CCTAAGAGTG TAGAAGCCTG ATGAAGGGGC TTGACTGGCA 420
GCTGCTTTAG CCTTCCTCTC TCAAGCCCCA GGAGAGGAAG CATTCAGCAC AGGCTGACTG 480
TGACTAGACC AGAAAAGCCA ACCGTCCCAC TGCAGGGGCC TGAGCCTTTT CTGCTATGTG 540
GGTGGAGAAA GTGAAGCTTC CCCACTGGTT TCCTGGGAGA TACAAGATAA GTGGTGCAAG 600
AAGTGCATGC AGAAAGGGAA GGAGTTGAGA GACTGGGGGG AAGAGAGGCC AGGTTAACCA 660
ATGCACTGAA CTCTTACCTA TTCTCAAAGA AAACTGTCAT ATTAGCCTCC TCCCTCCCCG 720
CAAGTGCTAC CTAAGAGGAG CCAGGGTAAG TGCTGCAAGG CATGGCAGAC AAAATTGCAC 780
ATCTTGGCCA GAATCTAAGG AACTTCTTGT GGTTTGGGGG AGGTGGTGAG GATGTGGGTG 840
GTGGGTGGGT GGGGGGTGTT GAAGAGATGC AGCCATGGAC TTCCTTGGGC TTGGCACAGG 900
CCAAAACAGA AGAGAGAACT CCAAACTCCA AGTAGTCCTC ATCAGACTTG CTCTCCTTAT 960
CAGCTTCATC CTGTCAGCCA AATTGTCAGC CATAGAAAAA CTGCTTTGCA GATGAAAAAC 1020
|
