| Tag | Content |
|---|
EnhancerAtlas ID | HS093-15478 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:33770300-33772100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr19:33771628-33771642 | CTGAGTCATTTTCT | - | 6.51 | | NFE2L1 | MA0089.2 | chr19:33771624-33771639 | TTAGCTGAGTCATTT | - | 6.35 | | ZEB1 | MA0103.3 | chr19:33770901-33770912 | GGGCAGGTGGG | - | 6.14 | | ZNF740 | MA0753.2 | chr19:33771276-33771289 | ACGCCCCCCCCAA | + | 6.05 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09601 | chr19:33770569-33772283 | CD14 | | SE_23808 | chr19:33771609-33772766 | Colon_Crypt_2 | | SE_24807 | chr19:33770396-33771226 | Colon_Crypt_3 | | SE_24807 | chr19:33771482-33773235 | Colon_Crypt_3 | | SE_27669 | chr19:33770580-33771220 | Fetal_Intestine | | SE_31890 | chr19:33770314-33771349 | Gastric | | SE_35421 | chr19:33764588-33771627 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I033277 | chr19 | 33768840 | 33771906 |
|
Enhancer Sequence | GATTACAGGC GTGTGCCACC ACACCCAGCT AATTTTTTGT ATTTTTAGTA GAGATGGGGG 60
TTCCCCATGT TGGCCAGGCT GGTCTCGAAT TCCTGTTGAT TCTCGAATTC CTGGTGATCC 120
ACCTGCCTTG ACCTCCCAAA GTGCTGGGAT TACAGGTGTG GGGCATCACG TCCGGCACTT 180
CCCATGCTCT CAGAGCATTC ACTGCTGCTG TCCAGGTCAG AGTCTGCCAG TGCCCTCCTC 240
CAGGAAGCCC ACCTGGGCTG GACCAGAAGA GGCAGGAGCC TGAAGCAGCC GGCCTTCCTC 300
CCCACCACAC ACCGGGACCG GGGCTTCCCC TCGCCACACT GATTAGGCTG GAAGTGGGGG 360
GCTTCCAGCT TCCCACTTCT GGAAGACCCC ACCTGCACCC AGCCTGCCTG GGGCTCAGGG 420
CTGCATTGAA AATGCCTGAC TTTCCACCCC AGAGTCCAGG GCAAGGCACA GCTTCTGATA 480
ACCCCTGGGC TGATGTTTGA GCAAGGCCCC TGGGAAAAAG TCCTCAGGCC TTACTGAGCC 540
CAGTGCTGCC GCTGTTGCTA CAGCAGACAA CCTGGGGCAA CGTCTCCGGA AGCTGGAGAA 600
CGGGCAGGTG GGGCAGCCAC AAAGAGGGCT CCAGCGGTGT CGGCTGCCTC GGTGTGCGGT 660
TCACTGTGGC TGTGTCCACC TGCTGCCTTC CTCTCTGGGC ACTTCCACTG ATATCTGGGA 720
GGAGGCCACC TCCAGGGGTT GTGAGCACTC AAATGAGACA ATGTGGGCAA GTGCCTGGCC 780
TGCTGCTTGG CGCACACTGA ACCCTCAATG AATGCAGCCA TCAGCCCTGC TCAGGCTGGC 840
AGGGTTGTGA GGACTGGAGG ATCCAGGTCA TCTCTGCAGA CCAGGGCAAG GCCTACTGCT 900
GGACAAGGGG AAGGCTTGGG ACTAAATCTC TGCCTTCCTG GCCCCCAGAG TCCACAAGGC 960
ACAAATGTGC ACTTGCACGC CCCCCCCAAC ACACATACAC ACACACATAC ACACACACAC 1020
ATACACATAC ACACACACAC ATACACATAC ACACACACAC ACACACACAC ACACATACAC 1080
ACATACATAC ACATACACAC ACACACATAC ACACACACAC ACCTGGCTTG GCTTCCCATT 1140
ACCCAGCCAC CTGCTGGAAA ACCAAGAGCT GTCTCTTGAA AAGGATGATT AAGAACCAGC 1200
CTTGACTACT CAAACTGAAA CTCCAAACCC TCCTCTGGGG TACCCAGCTC CTCTGGAGCC 1260
TGTGGGCGAA AAGCTCTTAC CATAGTGGAA AAAATATTCT GCCGAAACGG AAGTCTTCCT 1320
CAATTTAGCT GAGTCATTTT CTTGTGGTTA AGGAAGTCCG GGTTACCTCT GGCCCTTCCC 1380
CTGATGCCCA TGGCCTAGCC AGCTTGGGGG ACCCCAGTCC ACACTCCCGC CCTGGCAGGG 1440
GGCATGCCCA TCCCGGCAAA CCTGCAGGGC CCTTGATTGT AAGTCACCCC ACTCACCCCG 1500
GGCTGCTTCT CACCACTGTT TCCTGTGCTG AAGTGGGAGT CCAGACCCCC AAGAACCAGG 1560
ATCCAGGGTC ACTGATCACC AGGTCACCAG GGGCAGCTCC TACAGGCCTG GGGTCTGCCT 1620
GCGCTTCCTG TCGGGGATGG TGGCCCCTTG AGGATAGAGG CCTCCTGTGG ATTGACACTC 1680
TGCTCCTGTG TCCCCAGCTT GGGCAGCTCT TAGCACGAGG TCGGTATCAG GAGCCCAGTC 1740
TCCCAGCATT CAGCAGCTCA CAGATCCCCC AAGGAGCCGG TAGCTTGGAA TGAGTTCCTA 1800
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