| Tag | Content |
|---|
EnhancerAtlas ID | HS101-30602 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:126728570-126730800 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr3:126729980-126729991 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr3:126729980-126729991 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01881 | chr3:126726131-126732836 | Aorta | | SE_68930 | chr3:126727317-126729347 | H9 | | SE_68930 | chr3:126729534-126731600 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I127007 | chr3 | 126726132 | 126732836 |
|
Enhancer Sequence | TCTTGTGCCT GCCTGCATGC TGGGGTCTGT GTGTTTTGTC TGAAGGCGGA GTGGCCTGTG 60
CATGTTGATG GGAAGGGCCG CCAGACTGGG GCCATGGAGG CAGCTGGTGC TGTGTGCCAG 120
GGCCTAAGGG CTCCCACGTG GAGCCCCCAC CGAAGCTGAG CTCATGAGAC ACGCTGAGAA 180
GTCGGGACTT TCTCTTAGAA ATGCCTGTTT CTGGACTCTG CAGAAAGGGA GGAGTGTGGT 240
TCGTGTCTTC ACATAACAGT TGCATGCCCC GCCAGTCAGC TCCCAGATCT GAGCAAGTCT 300
ATAGACTCCT TGCTTGAAGG AGAGGCTGGG GTCCCTTGAG GAAGGAGCCT TGTGCGCTGG 360
CAAAATGCAC CCTGTTAATC TTCCCCCAGC GTTTCCCAGA GGGACCTCCA GCCTTTTACC 420
AGGGAGACTA TGCACTGGGG AGAAGGTTGT AATCGGAGCC TTTGGGGACA ACCGGACCTG 480
GCTCTGAAGA AGGACCTCCA GCCTTTTACC GGGGAGACTA TGCACTGGGG AAGAGGCTGT 540
AATCAGAGCC TTTGGGGACA ACTGGACCTG GCTCTGAGCT GTCATTGATC CCAGGAGACC 600
CACGCCACTG CAGGCCTCCT GTCAGAGTCA GAGTCAGGCC AGGTCGAGTC AGGTGATCAC 660
TGGAGTTTCA GCCTAATCCT GACTCAGTGG GCCGCATGGG TGCCGAGCTT CCTGGGTTCT 720
CACTCAGCTG GGTGTTGGGG AGGAGATGGG GTGGGGGTAT GGGGAGCACC TGAGAGGACC 780
GGGTGTGGCC CAGGCAGCCA GTCAGCTTCC TGCACCTGGC AGAGGGCAGG GGTGGCGAGG 840
GGACAGGCCA GCTTCAGGGT GATGGGGCAG GCAGGTAGGG GCCAGCCACA TTGGCCTTGA 900
TGCGTGCTGG GCCCACACGC TCACACTGGT GTTGGGGTGG GTGGTGCTTT TTCCTGGCTG 960
GGACCTGGGT TCTGGGGGTG GGCCATGACT GAGACCTCAC GCCAGGTGAG CCAGCTTCAT 1020
GTCTCGTGCT ACCGGCCAAG AGGTTTCCTG AACTTACGGG CACCAACAAA GCCCGTCCCT 1080
CACCATAGTC ACCTTCTGGC TTGCTGCAGG CTGAGCTGCC TGGGCTCCTC TGGGCATTTT 1140
TCAGTTGGTT GGATGGTGGG GGCAGCTCAG CTGGTCTCAG ACTGACCATT CTCGGGCGCT 1200
CACGGGCAGC CTAGCTTGGA CTGAAAGGAG TCTCAGTGCC CTGAGCCACC CGTTTTCATG 1260
GCTGGGGCCC TAAGGTGACA AGGCCCACGG TGGCCCGTGT CACGGTGAGA CTCCAGCCTG 1320
AGCCTCAGCA TGCAGAGTCA CTGGGCGCGC CTCAGACTGC CAGGGAGGTA CAGCATAGGT 1380
ATGGCCACTG TGCGTGCCTG TGCCTTCCGG CTGCAGCTGT TCTGGGAACA CAGAGTTGCA 1440
AGTGCAGCCC CTAAGTTGGG GCCAGTGGCC CTAGCTGCAA GGTGCCACCA CCTGCCTCTC 1500
CCCAGTGGAC ACAGGAGCAT CCCTGCAGAC CCAGAGATTA GTGGTCATCT TGCCCAGCTG 1560
GGCCTTGTTA ACTCTGCTTC CCTGGAGCTC CTGAGGGGCC AGGCCAGAGT CCAGGCCCCC 1620
TCTTGGGTCC TGGAAAATCT CTGCAGAGCT GGGCCTGGGC CTTCCTGCCT GCCTTGGGGG 1680
CTGTTGCAGG GCTTGGGGAT TACAGCCTGT TTTCAGCATC CCTATTTAAA GCCCAGCTTC 1740
TCAGTGTTCC CGAGGGGCCA TCTCCTGAGG CCAGCAGCAG CCATGCTGCA AGGAAGCCAG 1800
GCCATTGCAT CAGTTATTGT TGCCGAAATG CTGGCCCCAG AGGCCAGGCC TGTTTTTCTG 1860
CTGGGCTCTG GCTATTTTTA TACACTCCCT GGGCCCCCAG CGCAGAGCCT GCAGCCCCAG 1920
AGCCCCAATC TCTTCTGCCT CTGGGGCCTT TTCAGCTGCT GGCCAGATGG GGCTCCTTTG 1980
GTCTCTGGAA TGGTGGGGGT CCTAGAACAT GGGGCAGGGC ATTCAGGGGC CAGAGGTAAT 2040
AGAGCCTGTC TGGGTCATAG TATGCAGTCA CTGTCCCAGC CAGCGGTCCT CAGTTTGCCA 2100
GTGCATAAAA TGGGCACATT GGTGCTTGGC TGGGAGCACC ACAGGCCCAG TGCACATCTG 2160
GAGCGTAGTG GGGTGCACCT TGCTCACTGG TCTCCGCCCC CGGGCTCAGC CAAACTCTTC 2220
TTATCCCCAG 2230
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