| Tag | Content |
|---|
EnhancerAtlas ID | HS073-07592 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:33770420-33772740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr19:33772638-33772648 | GGTCACGTGC | + | 6.02 | | JUN(var.2) | MA0489.1 | chr19:33771628-33771642 | CTGAGTCATTTTCT | - | 6.51 | | NFE2L1 | MA0089.2 | chr19:33771624-33771639 | TTAGCTGAGTCATTT | - | 6.35 | | NFIA | MA0670.1 | chr19:33772426-33772436 | GGTGCCAAGT | + | 6.02 | | 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 | ACCTGCCTTG ACCTCCCAAA GTGCTGGGAT TACAGGTGTG GGGCATCACG TCCGGCACTT 60
CCCATGCTCT CAGAGCATTC ACTGCTGCTG TCCAGGTCAG AGTCTGCCAG TGCCCTCCTC 120
CAGGAAGCCC ACCTGGGCTG GACCAGAAGA GGCAGGAGCC TGAAGCAGCC GGCCTTCCTC 180
CCCACCACAC ACCGGGACCG GGGCTTCCCC TCGCCACACT GATTAGGCTG GAAGTGGGGG 240
GCTTCCAGCT TCCCACTTCT GGAAGACCCC ACCTGCACCC AGCCTGCCTG GGGCTCAGGG 300
CTGCATTGAA AATGCCTGAC TTTCCACCCC AGAGTCCAGG GCAAGGCACA GCTTCTGATA 360
ACCCCTGGGC TGATGTTTGA GCAAGGCCCC TGGGAAAAAG TCCTCAGGCC TTACTGAGCC 420
CAGTGCTGCC GCTGTTGCTA CAGCAGACAA CCTGGGGCAA CGTCTCCGGA AGCTGGAGAA 480
CGGGCAGGTG GGGCAGCCAC AAAGAGGGCT CCAGCGGTGT CGGCTGCCTC GGTGTGCGGT 540
TCACTGTGGC TGTGTCCACC TGCTGCCTTC CTCTCTGGGC ACTTCCACTG ATATCTGGGA 600
GGAGGCCACC TCCAGGGGTT GTGAGCACTC AAATGAGACA ATGTGGGCAA GTGCCTGGCC 660
TGCTGCTTGG CGCACACTGA ACCCTCAATG AATGCAGCCA TCAGCCCTGC TCAGGCTGGC 720
AGGGTTGTGA GGACTGGAGG ATCCAGGTCA TCTCTGCAGA CCAGGGCAAG GCCTACTGCT 780
GGACAAGGGG AAGGCTTGGG ACTAAATCTC TGCCTTCCTG GCCCCCAGAG TCCACAAGGC 840
ACAAATGTGC ACTTGCACGC CCCCCCCAAC ACACATACAC ACACACATAC ACACACACAC 900
ATACACATAC ACACACACAC ATACACATAC ACACACACAC ACACACACAC ACACATACAC 960
ACATACATAC ACATACACAC ACACACATAC ACACACACAC ACCTGGCTTG GCTTCCCATT 1020
ACCCAGCCAC CTGCTGGAAA ACCAAGAGCT GTCTCTTGAA AAGGATGATT AAGAACCAGC 1080
CTTGACTACT CAAACTGAAA CTCCAAACCC TCCTCTGGGG TACCCAGCTC CTCTGGAGCC 1140
TGTGGGCGAA AAGCTCTTAC CATAGTGGAA AAAATATTCT GCCGAAACGG AAGTCTTCCT 1200
CAATTTAGCT GAGTCATTTT CTTGTGGTTA AGGAAGTCCG GGTTACCTCT GGCCCTTCCC 1260
CTGATGCCCA TGGCCTAGCC AGCTTGGGGG ACCCCAGTCC ACACTCCCGC CCTGGCAGGG 1320
GGCATGCCCA TCCCGGCAAA CCTGCAGGGC CCTTGATTGT AAGTCACCCC ACTCACCCCG 1380
GGCTGCTTCT CACCACTGTT TCCTGTGCTG AAGTGGGAGT CCAGACCCCC AAGAACCAGG 1440
ATCCAGGGTC ACTGATCACC AGGTCACCAG GGGCAGCTCC TACAGGCCTG GGGTCTGCCT 1500
GCGCTTCCTG TCGGGGATGG TGGCCCCTTG AGGATAGAGG CCTCCTGTGG ATTGACACTC 1560
TGCTCCTGTG TCCCCAGCTT GGGCAGCTCT TAGCACGAGG TCGGTATCAG GAGCCCAGTC 1620
TCCCAGCATT CAGCAGCTCA CAGATCCCCC AAGGAGCCGG TAGCTTGGAA TGAGTTCCTA 1680
GTGGATGGGC AGTGGAGGGG CTGGGTGCCA GGCCCTGCTT AGATCTCAGA CCCAGTTGGG 1740
CTCATGGCAA CCAGGGATGG AACCTGTTTC ATTCTGGATC CTAGGAGTCT GAGCCTGCAG 1800
GCCAAGGCAC CTGGCCCAGG TGTGGCAGAG CCTTGCCCAG TCGGGGCTCT GGCTGGAGGG 1860
AGGCTGGTGC TGGTGGGTGC CCCACCCTGG CTGCAGGTGG CTGCCTCCTC CCCGGGAGAC 1920
CTTTTGGAAG GTGCCAGAGG CTGTTGTGGG GGAAGGCGGA GAGATGACGG GGCGGGCCAC 1980
CTGAGTGCCG TGGGGAGAGC CTTGAAGGTG CCAAGTGGTG CCAGTTGCAG GTGGGGCGTG 2040
GAGGCCAGCT CTGTGGGCGC TGGGTCCTTC CCCTGCGGCC ACACCGTGTG CCAGGAACGA 2100
GAGACCCCCT GGCTGTGCGT TCCACCCTGG CCCTCCATCT GAGCCCTGGG CTACTGGGGA 2160
GGCAGCAGGA GCCCGGGCAG ACGGCTCATC TGAGCTCGGC CTTCTGTCAG CTGACAGGGG 2220
TCACGTGCTG TCTGGGCTTG CCTGGGGCCT GAGAAATGGG GATGCGGACA GCCATTGTCA 2280
GGGCTGTTGG GGAAATTCAA GGAATGGAAG AGTCAGAGGG 2320
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