Tag | Content |
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EnhancerAtlas ID | HS093-14330 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr18:46518550-46519870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPIC | MA0687.1 | chr18:46519286-46519300 | TACTTCCCCATTCT | - | 6.45 | ZNF263 | MA0528.1 | chr18:46518868-46518889 | CCCTCCTCTGCCTCCTGCCTC | - | 6.24 | ZNF263 | MA0528.1 | chr18:46519563-46519584 | TCATCTTTTCCCTCCTCCACC | - | 6.53 | ZNF263 | MA0528.1 | chr18:46519560-46519581 | CCCTCATCTTTTCCCTCCTCC | - | 7.93 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_35081 | chr18:46516237-46521361 | HeLa | SE_46295 | chr18:46518915-46525824 | Osteoblasts | SE_53633 | chr18:46518612-46521698 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I048987 | chr18 | 46514328 | 46525924 |
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Enhancer Sequence | AGGAATAGAG GCTCACCTCA TACCTGCCCC ACAGCCTCAA GCTCGGGTCA GACATGGAGG 60 AGGGCATGGG TCTGGCTCCT CCCCTCTCCT TGTCCAGCAC TGGCCGGATG GTGTCCCCCG 120 CCTGGCACTA TCGCGGCAAC CATGTTCCTG GCAGGAGGAA GTGTGGCAAT TGCTGGAAGG 180 GCCAGTCTGC AGGCCAGGCC AGCTGGGGTG TCCCCTTCTT CACTGAACAG GCCTCTTCAT 240 GGCCTCCAGC CTCATTTGCT GTCATCCAGT GGCCGCTTTT CAGGCCCTCT CTGGGTGATG 300 TTGATGCCAT GGACCGTCCC CTCCTCTGCC TCCTGCCTCA TCTTCTAGAA CACTCCCCAC 360 TCCCCCAACT GTCCTCTCAG TGGACTCCTC AGTCTCCCCT GCCACTTGCC CCAAATGTGG 420 GTCCCCTGGG GACTGGCCTC AGTACTGTCC TCGCTCCACA TTCTCCAAGG AGTGACTTCA 480 CCCAAACCAC GGTTTCAAAT GCTATCTGTG CCCAAGGCCT CTCGAGCCCG GACCTCCTTT 540 CTGAATTCCG GACCCCTCAC CCAGCTGCGT GTAGACCCTC TCTCCAGGCA CAGCCCCAGC 600 CTGGCCACAC TCAGTCTGCT CCTGCTCTGG TTTTCCCAAT GCACAAATGA CAGCGTCATC 660 CGACAGATTT CCTCAACCTT GTCCTTGACT CCTTCCTGCC CCCACCCCTA CTAACTTCAT 720 GGCTGATTTC AGCACTTACT TCCCCATTCT GTCTACTGCT CTCCACCTCC CTCCACCAGC 780 CTGGGCCAGG CATTGTCATT TGTCACCAAA CCACTGCAGC CATCTGTTAA CTTAATGTCA 840 CACTGCCACG CTCATCCACC TTCAAGCCTT CATACCCCGC CTTGGGAAGT CTGAAACAGG 900 GGAGCCTGGG TGTGCCACAT TCCTGCCTAA CTCCTCCCAT CGCTTCCCAC TGCTCTAGGA 960 CAGAGTCCTC TGGAAGGAGG CTGACCTTCC TTCGTCCTCG CTCCCATCTG CCCTCATCTT 1020 TTCCCTCCTC CACCCACATT CCAGCCATTA TTCCCTGTCT GCTCAGAGTT TCCCAACATG 1080 TTGGGATTGA TCCCTCTGAG ATGTCCACCT GCTCTAGAAT GCCCTGCCTC CTTCCTCCAG 1140 CAAACTCCTA TTCATTCCTC AAAACATCAT TCGTGTGCTA CCTCCCCTGG GAAGCCTTCC 1200 AGGACTTCTC AGTCTTTGTG TGGTAGGGAC TTAGAACGGG TCTTGGTGTT TCACAGTGCA 1260 GAACACAGTT TCTGCTTGAG CTTTCAAGGC AACGACTTTT TCAGTTGCCG TGACCATGGG 1320
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