Tag | Content |
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EnhancerAtlas ID | HS105-29305 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr16:387810-388640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr16:388336-388349 | AGAAACAGCTGCT | - | 6.28 | RREB1 | MA0073.1 | chr16:388430-388450 | TCACAACCCACCCACACAGC | + | 6.12 | Tcf12 | MA0521.1 | chr16:388339-388350 | AACAGCTGCTG | + | 6.32 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25025 | chr16:387390-388026 | Colon_Crypt_3 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 387964 | 388479 | chr16 | 387937 | 388610 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I000337 | chr16 | 387643 | 391081 |
|
Enhancer Sequence | TGGGCCCTAT GGGCACTCAG CCGGGCGTGC GGCCTCTGGG GGCCCCCTGG ACGCCACAGC 60 AGTATGGCAG AGCTGTGTGT GTTTTCACAG AGCCCTGTGA CCAGTCTCCA TCTCTCAGGG 120 AGTGGAGAGA CCGAACACCT TCTGGAGCTA ATGGGTTCTG AGAGAACCCT GAGTGGTTAT 180 TCTCACAGAT GTGACACGGG GAAAAACTGA GGTGAAGCTG CTTCCCTCCA CACGCACAAG 240 TAGGCAGCGG AGGGGCCCAA GAAAGAGCCA ACAGGCGGCC CTCTCTCCCT GACAGCCACC 300 ATAGCCCAGC CTGGCCCCCA CCTCCGATAA CTGCAGGGTA CGCTGCTACA AATGACGTCT 360 GCGTTTGACA AGGATGAGCA GAACCGGAGC GTGTGCGTCA ATTCAAATCT GTGACACTGG 420 CGCAAAATGT GAGAATGGGC TGGGGTGCCA GGCGGCCAGT CACGGCTAGG GCACAGTTCC 480 AAGAAGGGCC ACAGGGGCCC GCAGGGACAC TTACCCCAAG CCCTCCAGAA ACAGCTGCTG 540 CAGGTCAGCA CCAGCACCAG GGCCAGGCAC ACAGTCTCAT CGGCACGTCT GCCACTGGCT 600 GTCTGCAAAG TGCTTCCCTT TCACAACCCA CCCACACAGC TCAGGACTGA GGTCCGCCCA 660 GGCAAAGGGG CCTCTCGGTT CCAGAATCCT TTGGCCTGAC AGGCAACTAC AGATACTTTC 720 GTGGACTCTG CTGAAACCTG TCTGAGACTA TGGAGCTTTA CGTGGCTAAG GAAGAGAAAA 780 AATATGTTTG GAGTCCTTGC CCACTGACAG GTGCATAAAA ATACAAGATG 830
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