| Tag | Content |
|---|
EnhancerAtlas ID | HS077-05080 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr17:79694150-79695230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | | FOSL1 | MA0477.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.62 | | Foxd3 | MA0041.1 | chr17:79695167-79695179 | GTTTGTTTGTTT | + | 6.32 | | JUND | MA0491.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr17:79695075-79695090 | TGAACTCTTAACCTC | - | 6.53 | | TFEB | MA0692.1 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | | YY1 | MA0095.2 | chr17:79694583-79694595 | GCAGCCATCTTG | - | 6.74 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24622 | chr17:79694215-79694862 | Colon_Crypt_2 | | SE_24986 | chr17:79694274-79694842 | Colon_Crypt_3 | | SE_27510 | chr17:79694061-79695025 | Esophagus | | SE_41699 | chr17:79694211-79694856 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I081727 | chr17 | 79694338 | 79695210 |
|
Enhancer Sequence | CCAGCCTGGG CTACAGAGCT AAACTGTCTC AAAAATAAAT AAAGTAATAA AATAATAAAA 60
TAAATAGTCA CGTGATGCTT CAGGTCATCT GACATCCTGC CCCCCACCCC TTAGTAAAAT 120
GCCTGCTGTT TTATTCAAGC AGCTACCACC CCACCCCAGT CCTTGGGCCT CAAGGGCACC 180
AGGGCCTGAC CCCAGCTCCC AGCATGAATA GGGTTGGTTT AAACCAGTCG GCATGGCCCA 240
CAGTGACTGG TTTAGGCATG GGCCTGTCAC CCACACTGGG CCAATGATAT GTAAGATGTT 300
TATTGTAGCT TCCGGGATGG AAACTTCTCT GCCAGCTTGT GGGTTGGGCA AGGACGACAC 360
TCCGGGCCCT ACCGGCGGAA GCTCTGCTCC TGTCGTGCGT GGACCACGCA GCAAATGGCC 420
TTGGAGGCTG CTGGCAGCCA TCTTGTGACC ATGAGGCAAG TCAGCGCAGG CCGAAGCTGA 480
CGACGCGAAG ACAATGAGGA GAGGGAGAAA GAGCCGATCT TTGGTGTGTA TTGGCTGTGA 540
CGTGCTGCCG CCTCTCTGGA GACCGGGTTC ATTATACTTT TCCTGGTATC TTCTCATGTT 600
TGCTCTGCTG GCTTTGGGCC CGAGTTTTAC CTCCTGGGTG TATTGTGTGT GCCTGTTTTG 660
TGGTGTTGGT TTTGCTCCTG GGTTTGTTGA CCCTTGGGTG TCTGCTCTTT TTTTTTTTTT 720
TTTTTTTTTT TGGGACAGAG TCTCACGCTG TCACCCAGGC TGGAGTGCAG TGACCTGATC 780
TTGGCTCACT GCAGCCTCTA CCTCCTGGGT ACAAGCGATT CTTCTGCCTC GGCCTCCTGA 840
ATAGCTGGGA TTACAGGTGC CTGCCACGGC TAATTTTTTT ACTTTTAGTA GAGATGGGGT 900
TTTGCCATGT TGGCTAGGCT GGTCTTGAAC TCTTAACCTC AGGTGATCTG CCCACCTCCG 960
CCTCCCAAAG TGCTAGGATT TATAGGCATG AGTCACCGTA TCCAGCATTT TTTGCTTGTT 1020
TGTTTGTTTT GAGACGGAGT CTCGCTGTGT CACCCAGGCT GGAGTGCAGC GGTGTGATCT 1080
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