| Tag | Content |
|---|
EnhancerAtlas ID | HS093-11489 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:23874580-23875720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF8 | MA0652.1 | chr16:23874937-23874951 | AGTTTCATTTTCGT | - | 6.01 | | IRF9 | MA0653.1 | chr16:23874937-23874952 | AGTTTCATTTTCGTA | - | 6.02 | | SPI1 | MA0080.4 | chr16:23875259-23875273 | TAAAAGAGGAAGTT | + | 6.83 | | SPIC | MA0687.1 | chr16:23875259-23875273 | TAAAAGAGGAAGTT | + | 6.34 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_10067 | chr16:23863461-23878484 | CD14 | | SE_10888 | chr16:23856132-23883188 | CD20 | | SE_32644 | chr16:23868998-23876906 | GM12878 | | SE_60111 | chr16:23838010-23894131 | Ly4 | | SE_63093 | chr16:23837102-23894105 | Tonsil | | SE_67999 | chr16:23846983-23921777 | TC32 |
|
| | 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 |
| GH16I023855 | chr16 | 23866922 | 23876752 |
|
Enhancer Sequence | ACACACACAC ACACACACAC ACACACGAAT ATTTTACCTA GGGTGGACGT GCTCCTTCTC 60
TTACTTTTAG GAACCCCCTA CTCTGTCTAT GGAGTAACTG TTCTTTCACC ACTTTACTTT 120
CTTAATAAAC TTGCTTTTGC TTTGCACTGT GGACTCACCC TGAATTCTTT CTTGTGCAAG 180
ATCCAAGAAC CCTTTCTTGG GGTCTGGATC AGGACTCCTT TCCTGTAATA CAATGTCACA 240
GAGCTCTTAA GTGGCAGAGC TTGGGGCCAA ACTTAGGCTG CTGCACCCGA TGTCCCAGCT 300
CCTCTGCCCT ATCTAGCTGT GGATTTGTGC CTCGAAATAG AATTGCATTT TGAATGCAGT 360
TTCATTTTCG TATGGAAAGT GTCTATCCTG TAAATGTAAC TGTAGCAGCC CCAAAGCTGA 420
GCTGGGCAGT TTTATGGCAG CCTGGAGTCA GTCTTGTCCG CTTCCAATCA GGGTTCCTGG 480
ACTGGCTCCT ATATTAAAAT TGGTATTAGT AGACAATGTT CCAGGCAGAG TTTTGGATAG 540
AAACTATCCA TCAGCACCAA GAATGTGCCT GATTTGGTAA TCTTTTTACC AAAGTAAAAG 600
TCAGTAGTAA GTTGTGGTTA AAAGAGAGGA AGTTCAGAGT TCAGTACGTT ATTTCTCTCT 660
CTCTCTCTCT TTGTTTAAAT AAAAGAGGAA GTTACTGCTC TTATTTTTGT ACCAGCCCGT 720
CAGTAATGGG TACAGAGTAA AATCTTAGCT AAGCTGAGGT CAAACTTCAA AACTTAGTAA 780
TAAGGATCTC CCTTGTTCCT TTGTAGGGCG ACTAACATGA AGGTTCTGAC TCTTAACCCA 840
TAGAGCCACA AAAAATAGTC CTAGGAAAAT CATATGATTT TATTTATTTT AGGAACAGAA 900
ATGGTCCCTT CCGAAGTAGA GGCATTTCTA CTTCTTTCCT AAACACCATC TCTGCTCAGT 960
GAGCTCTCCC ACCCTCAGGT ACTGTGTTTC AGGCTTATTG CTGTATTGCT AGAAGTATCC 1020
TCACCTTCGA GATTAAGAAA AGATATTTAT TGCCGGGCAC AGTGGCTCAC GCCTGCAATC 1080
CCAGTCTTTT GGGAAGCTGA GACGGGAGGA TCACTTGAGC CCAGGATCTT GAGACCAGCC 1140
|
