Tag | Content |
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EnhancerAtlas ID | HS093-23533 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr4:40674530-40675740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr4:40675086-40675097 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr4:40675086-40675097 | CTGAGTCATCC | - | 6.14 | NFE2L1 | MA0089.2 | chr4:40675082-40675097 | AAAGCTGAGTCATCC | - | 6.45 | Nfe2l2 | MA0150.2 | chr4:40675084-40675099 | AGCTGAGTCATCCTT | - | 6.06 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33946 | chr4:40673626-40676306 | HCC1954 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 40674578 | 40674731 | chr4 | 40674929 | 40675349 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I040670 | chr4 | 40672919 | 40676225 |
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Enhancer Sequence | CATGAACTAG AGAAAGAATA TTCCACGCCA AAGAGAACAG AGGCACAGTG GCCCAAGGCA 60 GGCAGGAGTT TAGCATAACT CAAGGGAGGG TCCAGAGGTC CTGCGGCTGG AGTGGAGTGA 120 GCCGGAAAGA GGAAGGAAAG GTCACATGAA GAGCTGGGGC CAGGTCCTGA TGGTAAGTGC 180 TCTTTGGAAC TCCTCCTTTT AAAACTGGCG TGTCTTCAGG AAGCTGAATA TCTACAAAGC 240 TAGGCCTCGG AGAGAAGGCT TTTCCTGAGT ATGTTTGTGT GAGTGATTCC GTGTGTTAAC 300 AAAGCGCCCC AGGATTTGCC TTTTCTTCCC CTGTTTCTTG CTGTTAGAAT GTTAATCTGG 360 CTAAATCCAT TCAGCTTCAC TCGTTTGGAA ATCAGTCATC TAATGCTTGT AGCGAAAAAA 420 GGAGACAAGC TAATACATCT CAACAGAGCA GATACGTGGG AGCCACTCCC ACAGATCAAG 480 ATCCTTGCAG AAACCCAAGC CATTGTTCAG CCAATAGTAA ATAAGAATCC GAGTCATTCT 540 AAAACTGAGT AGAAAGCTGA GTCATCCTTC CCTCTATCAA GAGCTTTATT CCTTTTGCAT 600 CCTGTGGATC TTGGTTGGTT AACACATTAC TGAATGGTGA CGTGGGTAGG TCTGTCTGCC 660 TGCATCAAAT CCTGCCCTAA CCACATTCTC AAGATAGTTT TCACCACATT TACTAAACTT 720 CCTTGAACCT CAGTTTCCTC CTCTGCAGGA GGAGGGTATG AATGCTTTAT TAGTTTTCTA 780 CTGCTGTGTA ATAAATTAGC ACAGATCTAG AGGGTAAGAG CTACTCCCAC TCATCATTTC 840 ACAGTGCTGT AGGCCAGAGG CCCCAGATGG CGTAACCAGG TTTTCTGCTA AGAGCCTTGA 900 AACGCTGAAA TCAAGATGTT GGTTGTCCGT GTCCTCACCT AGAGCTCAGG GTCTTCCTCC 960 AAGCTCATCC CTGTTGTCAG CAGAATGTAG GTTCCTGCAG TTGTGGGACC GAGGCCTTGT 1020 TTCCTCACTG GCTGTCAGCA GAGGCCATTT CTCAGCTCCT TAAGCCTGCC CCCTTCCTCC 1080 ACAGTGACCC TCTATTCCAA AGCAGCAACT ACACACCTAA CCCTTCTGAC ACTTGGAAAA 1140 CATCTGACTT CTGCTCTCAG CCAGAGAAAG CTCTCTGCTT TTATTCTTTT TTTTATCTAC 1200 TTATTTATTT 1210
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